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RANITIDINE
RANITIDINE - 55648-741-06 - (RANITIDINE)
Drug Information of RANITIDINE
| Product NDC: | 55648-741 |
| Proprietary Name: | RANITIDINE |
| Non Proprietary Name: | RANITIDINE |
| Active Ingredient(s): | 150 mg/1 & nbsp; RANITIDINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of RANITIDINE
| Product NDC: | 55648-741 |
| Labeler Name: | WOCKHARDT LIMITED |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA078653 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20071126 |
Package Information of RANITIDINE
| Package NDC: | 55648-741-06 |
| Package Description: | 6000 TABLET, COATED in 1 POUCH (55648-741-06) |
NDC Information of RANITIDINE
| NDC Code | 55648-741-06 |
| Proprietary Name | RANITIDINE |
| Package Description | 6000 TABLET, COATED in 1 POUCH (55648-741-06) |
| Product NDC | 55648-741 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | RANITIDINE |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20071126 |
| Marketing Category Name | ANDA |
| Labeler Name | WOCKHARDT LIMITED |
| Substance Name | RANITIDINE HYDROCHLORIDE |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
