NDC Code | 39822-5500-6 |
Package Description | 25 AMPULE in 1 CARTON (39822-5500-6) > 2 mL in 1 AMPULE (39822-5500-5) |
Product NDC | 39822-5500 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Promethazine Hydrochloride |
Non-Proprietary Name | Promethazine Hydrochloride |
Dosage Form | INJECTION, SOLUTION |
Usage | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20110502 |
Marketing Category Name | ANDA |
Application Number | ANDA040737 |
Manufacturer | X-GEN Pharmaceuticals, Inc. |
Substance Name | PROMETHAZINE HYDROCHLORIDE |
Strength | 25 |
Strength Unit | mg/mL |
Pharmacy Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |