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Ranitidine
Ranitidine - 76237-231-30 - (Ranitidine)
Drug Information of Ranitidine
| Product NDC: | 76237-231 |
| Proprietary Name: | Ranitidine |
| Non Proprietary Name: | Ranitidine |
| Active Ingredient(s): | 150 mg/1 & nbsp; Ranitidine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ranitidine
| Product NDC: | 76237-231 |
| Labeler Name: | McKesson Contract Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075165 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111026 |
Package Information of Ranitidine
| Package NDC: | 76237-231-30 |
| Package Description: | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-231-30) > 5 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Ranitidine
| NDC Code | 76237-231-30 |
| Proprietary Name | Ranitidine |
| Package Description | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-231-30) > 5 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 76237-231 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ranitidine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20111026 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson Contract Packaging |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |
