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PROMETHAZINE HYDROCHLORIDE
PROMETHAZINE HYDROCHLORIDE - 52125-529-52 - (PROMETHAZINE HYDROCHLORIDE)
Drug Information of PROMETHAZINE HYDROCHLORIDE
| Product NDC: | 52125-529 |
| Proprietary Name: | PROMETHAZINE HYDROCHLORIDE |
| Non Proprietary Name: | PROMETHAZINE HYDROCHLORIDE |
| Active Ingredient(s): | 25 mg/1 & nbsp; PROMETHAZINE HYDROCHLORIDE |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PROMETHAZINE HYDROCHLORIDE
| Product NDC: | 52125-529 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040737 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130411 |
Package Information of PROMETHAZINE HYDROCHLORIDE
| Package NDC: | 52125-529-52 |
| Package Description: | 25 INJECTION, SOLUTION in 1 CARTON (52125-529-52) |
NDC Information of PROMETHAZINE HYDROCHLORIDE
| NDC Code | 52125-529-52 |
| Proprietary Name | PROMETHAZINE HYDROCHLORIDE |
| Package Description | 25 INJECTION, SOLUTION in 1 CARTON (52125-529-52) |
| Product NDC | 52125-529 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PROMETHAZINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20130411 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | PROMETHAZINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
