Product NDC: | 55648-906 |
Proprietary Name: | RANITIDINE |
Non Proprietary Name: | RANITIDINE |
Active Ingredient(s): | 150 mg/1 & nbsp; RANITIDINE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55648-906 |
Labeler Name: | WOCKHARDT LIMITED |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075208 |
Marketing Category: | ANDA |
Start Marketing Date: | 19981217 |
Package NDC: | 55648-906-12 |
Package Description: | 5000 TABLET in 1 DRUM (55648-906-12) |
NDC Code | 55648-906-12 |
Proprietary Name | RANITIDINE |
Package Description | 5000 TABLET in 1 DRUM (55648-906-12) |
Product NDC | 55648-906 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | RANITIDINE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19981217 |
Marketing Category Name | ANDA |
Labeler Name | WOCKHARDT LIMITED |
Substance Name | RANITIDINE HYDROCHLORIDE |
Strength Number | 150 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC] |