Product Center-Guangxiang Technology_drug research & drug registration

Mecobalamin Injection

[Generic Name] Mecobalamin Injection

[Approval Number] National Drug Approval Number H20066715

[Specification] 1 ml: 0.5 mg

[Packaging Material] Glass Ampoule

【Dosage Form】Injection

Mecobalamin Injection

[Generic Name] Mecobalamin Injection

[Approval Number] National Drug Approval Number H20066715

[Specification] 1 ml: 0.5 mg

[Packaging Material] Glass Ampoule

【Dosage Form】Injection

Acetaminophen Mannitol Injection

[Generic Name] Acetaminophen Mannitol Injection

[Approval Number] National Drug Approval Number H20223397

【Specification】100 ml: 1000 mg

【Dosage Form】Injection

Acetaminophen Mannitol Injection

[Generic Name] Acetaminophen Mannitol Injection

[Approval Number] National Drug Approval Number H20223397

【Specification】100 ml: 1000 mg

【Dosage Form】Injection

Bunan Seline Tablets

[Generic Name] Bunan Seline Tablets

[Approval Number] National Drug Approval Number H20223407

[Specification] 4mg

【Dosage Form】Tablets

Bunan Seline Tablets

[Generic Name] Bunan Seline Tablets

[Approval Number] National Drug Approval Number H20223407

[Specification] 4mg

【Dosage Form】Tablets

Sodium Lactate Ringer's Injection

[Generic Name] Sodium Lactate Ringer's Injection

[Approval Number] National Drug Approval Number H20044961

【Specifications】500ml 1000ml

[Packaging Materials] Glass bottles, polypropylene infusion bottles, polypropylene infusion bags, upright polypropylene infusion bags, multilayer co-extruded film infusion bags

【Dosage Form】Injection

Sodium Lactate Ringer's Injection

[Generic Name] Sodium Lactate Ringer's Injection

[Approval Number] National Drug Approval Number H20044961

【Specifications】500ml 1000ml

[Packaging Materials] Glass bottles, polypropylene infusion bottles, polypropylene infusion bags, upright polypropylene infusion bags, multilayer co-extruded film infusion bags

【Dosage Form】Injection

Peritoneal dialysis solution

[Generic Names] Peritoneal Dialysis Solution (Lactate-G1.5%) Peritoneal Dialysis Solution (Lactate-G2.5%) Peritoneal Dialysis Solution (Lactate-G4.25%)

[Approval Numbers] National Drug Approval Number H20193081, National Drug Approval Number H20193085, National Drug Approval Number H20193080

[Specifications] Contains 1.5% glucose (2000 ml/bag), contains 2.5% glucose (2000 ml/bag), contains 4.25% glucose (2000 ml/bag)

[Packaging Material] Three-layer co-extruded film infusion bag for peritoneal dialysis, including a dual-bag accessory system for peritoneal dialysis.

【Dosage Form】Injection

Peritoneal dialysis solution

[Generic Names] Peritoneal Dialysis Solution (Lactate-G1.5%) Peritoneal Dialysis Solution (Lactate-G2.5%) Peritoneal Dialysis Solution (Lactate-G4.25%)

[Approval Numbers] National Drug Approval Number H20193081, National Drug Approval Number H20193085, National Drug Approval Number H20193080

[Specifications] Contains 1.5% glucose (2000 ml/bag), contains 2.5% glucose (2000 ml/bag), contains 4.25% glucose (2000 ml/bag)

[Packaging Material] Three-layer co-extruded film infusion bag for peritoneal dialysis, including a dual-bag accessory system for peritoneal dialysis.

【Dosage Form】Injection

Aggrastat Injection

[Generic Name] Aggrastat Injection

[Approval Number] National Drug Approval Number H20233354

[Specification] 2 ml: 10 mg

[Packaging Material] Type I borosilicate glass ampoules

【Dosage Form】Injection

Aggrastat Injection

[Generic Name] Aggrastat Injection

[Approval Number] National Drug Approval Number H20233354

[Specification] 2 ml: 10 mg

[Packaging Material] Type I borosilicate glass ampoules

【Dosage Form】Injection

Theophylline sustained-release tablets

[Generic Name] Theophylline Sustained-Release Tablets

[Approval Number] National Drug Approval Number H20233310

【Specification】0.4g × 10 tablets/box

[Packaging Material] Aluminum-plastic blister pack

【Dosage Form】Tablets

Theophylline sustained-release tablets

[Generic Name] Theophylline Sustained-Release Tablets

[Approval Number] National Drug Approval Number H20233310

【Specification】0.4g × 10 tablets/box

[Packaging Material] Aluminum-plastic blister pack

【Dosage Form】Tablets

Felodipine sustained-release tablets

[Generic Name] Felodipine Sustained-Release Tablets

[Approval Number] National Drug Approval Number H20223964

[Specification] 5mg × 24/box, 5mg × 48/box

[Packaging Material] Aluminum-plastic blister pack

【Dosage Form】Tablets

Felodipine sustained-release tablets

[Generic Name] Felodipine Sustained-Release Tablets

[Approval Number] National Drug Approval Number H20223964

[Specification] 5mg × 24/box, 5mg × 48/box

[Packaging Material] Aluminum-plastic blister pack

【Dosage Form】Tablets

Theobromine Injection for Ketones

[Generic Name] Theophylline Injection

[Approval Number] National Drug Approval No. H20223704

【Specification】5 ml: 0.1 g

[Packaging Material] Polypropylene Ampoule

【Dosage Form】Injection

Theobromine Injection for Ketones

[Generic Name] Theophylline Injection

[Approval Number] National Drug Approval No. H20223704

【Specification】5 ml: 0.1 g

[Packaging Material] Polypropylene Ampoule

【Dosage Form】Injection

Valsartan Amlodipine Tablets (I)

[Generic Name] Valsartan Amlodipine Tablets (I)

[Approval Number] National Drug Approval Number H20223692

[Specification] 3 ml: 0.5 g, 6 ml × 1 g

[Packaging Material] Aluminum-plastic blister pack

【Dosage Form】Tablets

Valsartan Amlodipine Tablets (I)

[Generic Name] Valsartan Amlodipine Tablets (I)

[Approval Number] National Drug Approval Number H20223692

[Specification] 3 ml: 0.5 g, 6 ml × 1 g

[Packaging Material] Aluminum-plastic blister pack

【Dosage Form】Tablets

Lipoic Acid Injection

[Generic Name] Lipoic Acid Injection

[Approval Number] National Drug Approval Number H20233115

【Specification】24 ml: 600 mg

[Packaging Material] Glass Ampoule

【Dosage Form】Injection

Lipoic Acid Injection

[Generic Name] Lipoic Acid Injection

[Approval Number] National Drug Approval Number H20233115

【Specification】24 ml: 600 mg

[Packaging Material] Glass Ampoule

【Dosage Form】Injection

Ornidazole Injection

[Generic Name] Ornidazole Injection

[Approval Number] National Drug Approval Number H13022514

[Specification] 3 ml: 0.5 g, 6 ml × 1 g

[Packaging Material] Glass Ampoule

【Dosage Form】Injection

Ornidazole Injection

[Generic Name] Ornidazole Injection

[Approval Number] National Drug Approval Number H13022514

[Specification] 3 ml: 0.5 g, 6 ml × 1 g

[Packaging Material] Glass Ampoule

【Dosage Form】Injection

Azithromycin Tablets

[Generic Name] Azithromycin Tablets

[Approval Number] National Drug Approval Number H20223821

【Specification】0.25g × 6 × 2/box

[Packaging Material] Aluminum-plastic blister pack

【Dosage Form】Tablets

Azithromycin Tablets

[Generic Name] Azithromycin Tablets

[Approval Number] National Drug Approval Number H20223821

【Specification】0.25g × 6 × 2/box

[Packaging Material] Aluminum-plastic blister pack

【Dosage Form】Tablets

Azithromycin Dry Suspension

[Generic Name] Azithromycin Dry Suspension

[Approval Number] National Drug Approval No. H20223641

【Specification】0.1g × 6/box

[Packaging] Composite film bag packaging

[Dosage Form] Dry Suspension

Azithromycin Dry Suspension

[Generic Name] Azithromycin Dry Suspension

[Approval Number] National Drug Approval No. H20223641

【Specification】0.1g × 6/box

[Packaging] Composite film bag packaging

[Dosage Form] Dry Suspension

Metronidazole Tablets

[Generic Name] Metronidazole Tablets

[Approval Number] National Drug Approval No. H13022514

【Specifications】0.2g × 12/box; 0.2g × 100/bottle

[Packaging] Aluminized plastic blister pack, plastic bottle

【Dosage Form】Tablets

Metronidazole Tablets

[Generic Name] Metronidazole Tablets

[Approval Number] National Drug Approval No. H13022514

【Specifications】0.2g × 12/box; 0.2g × 100/bottle

[Packaging] Aluminized plastic blister pack, plastic bottle

【Dosage Form】Tablets

Moxifloxacin Hydrochloride Eye Drops

[Generic Name] Moxifloxacin Hydrochloride Eye Drops

[Approval Number] National Drug Approval No. H20223142

[Specification] 5 ml: 25 mg

Moxifloxacin Hydrochloride Eye Drops

[Generic Name] Moxifloxacin Hydrochloride Eye Drops

[Approval Number] National Drug Approval No. H20223142

[Specification] 5 ml: 25 mg