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Ranitidine
Ranitidine - 49035-353-69 - (Ranitidine Hydrochloride)
Drug Information of Ranitidine
| Product NDC: | 49035-353 |
| Proprietary Name: | Ranitidine |
| Non Proprietary Name: | Ranitidine Hydrochloride |
| Active Ingredient(s): | 75 mg/1 & nbsp; Ranitidine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ranitidine
| Product NDC: | 49035-353 |
| Labeler Name: | Wal-Mart Stores, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA201745 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120710 |
Package Information of Ranitidine
| Package NDC: | 49035-353-69 |
| Package Description: | 10 TABLET, FILM COATED in 1 BLISTER PACK (49035-353-69) |
NDC Information of Ranitidine
| NDC Code | 49035-353-69 |
| Proprietary Name | Ranitidine |
| Package Description | 10 TABLET, FILM COATED in 1 BLISTER PACK (49035-353-69) |
| Product NDC | 49035-353 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ranitidine Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120710 |
| Marketing Category Name | ANDA |
| Labeler Name | Wal-Mart Stores, Inc |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Strength Number | 75 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
