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Ranitidine
Ranitidine - 21695-110-15 - (Ranitidine)
Drug Information of Ranitidine
| Product NDC: | 21695-110 |
| Proprietary Name: | Ranitidine |
| Non Proprietary Name: | Ranitidine |
| Active Ingredient(s): | 300 mg/1 & nbsp; Ranitidine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ranitidine
| Product NDC: | 21695-110 |
| Labeler Name: | Rebel Distributors |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077824 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091217 |
Package Information of Ranitidine
| Package NDC: | 21695-110-15 |
| Package Description: | 15 TABLET in 1 BOTTLE (21695-110-15) |
NDC Information of Ranitidine
| NDC Code | 21695-110-15 |
| Proprietary Name | Ranitidine |
| Package Description | 15 TABLET in 1 BOTTLE (21695-110-15) |
| Product NDC | 21695-110 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ranitidine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091217 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |
