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Promethazine hydrochloride
Promethazine hydrochloride - 54868-2088-0 - (Promethazine hydrochloride)
Drug Information of Promethazine hydrochloride
| Product NDC: | 54868-2088 |
| Proprietary Name: | Promethazine hydrochloride |
| Non Proprietary Name: | Promethazine hydrochloride |
| Active Ingredient(s): | 50 mg/mL & nbsp; Promethazine hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Promethazine hydrochloride
| Product NDC: | 54868-2088 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040737 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050929 |
Package Information of Promethazine hydrochloride
| Package NDC: | 54868-2088-0 |
| Package Description: | 25 AMPULE in 1 CARTON (54868-2088-0) > 1 mL in 1 AMPULE |
NDC Information of Promethazine hydrochloride
| NDC Code | 54868-2088-0 |
| Proprietary Name | Promethazine hydrochloride |
| Package Description | 25 AMPULE in 1 CARTON (54868-2088-0) > 1 mL in 1 AMPULE |
| Product NDC | 54868-2088 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Promethazine hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20050929 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | PROMETHAZINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
