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PROMETHAZINE HYDROCHLORIDE
PROMETHAZINE HYDROCHLORIDE - 57664-146-34 - (PROMETHAZINE HYDROCHLORIDE)
Drug Information of PROMETHAZINE HYDROCHLORIDE
| Product NDC: | 57664-146 |
| Proprietary Name: | PROMETHAZINE HYDROCHLORIDE |
| Non Proprietary Name: | PROMETHAZINE HYDROCHLORIDE |
| Active Ingredient(s): | 6.25 mg/5mL & nbsp; PROMETHAZINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PROMETHAZINE HYDROCHLORIDE
| Product NDC: | 57664-146 |
| Labeler Name: | Caraco Pharmaceutical Laboratories, Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040891 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090313 |
Package Information of PROMETHAZINE HYDROCHLORIDE
| Package NDC: | 57664-146-34 |
| Package Description: | 473 mL in 1 BOTTLE (57664-146-34) |
NDC Information of PROMETHAZINE HYDROCHLORIDE
| NDC Code | 57664-146-34 |
| Proprietary Name | PROMETHAZINE HYDROCHLORIDE |
| Package Description | 473 mL in 1 BOTTLE (57664-146-34) |
| Product NDC | 57664-146 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PROMETHAZINE HYDROCHLORIDE |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20090313 |
| Marketing Category Name | ANDA |
| Labeler Name | Caraco Pharmaceutical Laboratories, Ltd. |
| Substance Name | PROMETHAZINE HYDROCHLORIDE |
| Strength Number | 6.25 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
