Product NDC: | 0143-9868 |
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) |
Product NDC: | 0143-9868 |
Labeler Name: | West-ward Pharmaceutical Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040737 |
Marketing Category: | ANDA |
Start Marketing Date: | 20080424 |
Package NDC: | 0143-9868-22 |
Package Description: | 1 mL in 1 AMPULE (0143-9868-22) |
NDC Code | 0143-9868-22 |
Proprietary Name | Promethazine hydrochloride |
Package Description | 1 mL in 1 AMPULE (0143-9868-22) |
Product NDC | 0143-9868 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Promethazine hydrochloride |
Dosage Form Name | INJECTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20080424 |
Marketing Category Name | ANDA |
Labeler Name | West-ward Pharmaceutical Corp |
Substance Name | PROMETHAZINE HYDROCHLORIDE |
Strength Number | 50 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |