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promethazine hydrochloride
promethazine hydrochloride - 57664-109-83 - (promethazine hydrochloride)
Drug Information of promethazine hydrochloride
| Product NDC: | 57664-109 |
| Proprietary Name: | promethazine hydrochloride |
| Non Proprietary Name: | promethazine hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; promethazine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of promethazine hydrochloride
| Product NDC: | 57664-109 |
| Labeler Name: | Caraco Pharmaceutical Laboratories, Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040863 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090127 |
Package Information of promethazine hydrochloride
| Package NDC: | 57664-109-83 |
| Package Description: | 30 TABLET in 1 BOTTLE (57664-109-83) |
NDC Information of promethazine hydrochloride
| NDC Code | 57664-109-83 |
| Proprietary Name | promethazine hydrochloride |
| Package Description | 30 TABLET in 1 BOTTLE (57664-109-83) |
| Product NDC | 57664-109 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | promethazine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090127 |
| Marketing Category Name | ANDA |
| Labeler Name | Caraco Pharmaceutical Laboratories, Ltd. |
| Substance Name | PROMETHAZINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
