Product NDC: | 54868-1323 |
Proprietary Name: | Promethazine Hydrochloride |
Non Proprietary Name: | Promethazine Hydrochloride |
Active Ingredient(s): | 25 mg/1 & nbsp; Promethazine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-1323 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040863 |
Marketing Category: | ANDA |
Start Marketing Date: | 19950814 |
Package NDC: | 54868-1323-4 |
Package Description: | 15 TABLET in 1 BOTTLE, PLASTIC (54868-1323-4) |
NDC Code | 54868-1323-4 |
Proprietary Name | Promethazine Hydrochloride |
Package Description | 15 TABLET in 1 BOTTLE, PLASTIC (54868-1323-4) |
Product NDC | 54868-1323 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Promethazine Hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19950814 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | PROMETHAZINE HYDROCHLORIDE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |