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Ranitidine Hydrochloride
Ranitidine Hydrochloride - 68382-422-02 - (Ranitidine Hydrochloride)
Drug Information of Ranitidine Hydrochloride
| Product NDC: | 68382-422 |
| Proprietary Name: | Ranitidine Hydrochloride |
| Non Proprietary Name: | Ranitidine Hydrochloride |
| Active Ingredient(s): | 25 mg/mL & nbsp; Ranitidine Hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ranitidine Hydrochloride
| Product NDC: | 68382-422 |
| Labeler Name: | Zydus Pharmaceuticals (USA) Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091534 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130301 |
Package Information of Ranitidine Hydrochloride
| Package NDC: | 68382-422-02 |
| Package Description: | 10 VIAL in 1 CARTON (68382-422-02) > 2 mL in 1 VIAL |
NDC Information of Ranitidine Hydrochloride
| NDC Code | 68382-422-02 |
| Proprietary Name | Ranitidine Hydrochloride |
| Package Description | 10 VIAL in 1 CARTON (68382-422-02) > 2 mL in 1 VIAL |
| Product NDC | 68382-422 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ranitidine Hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20130301 |
| Marketing Category Name | ANDA |
| Labeler Name | Zydus Pharmaceuticals (USA) Inc. |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |
