NDC Code | 55700-221-20 |
Package Description | 20 TABLET in 1 BOTTLE (55700-221-20) |
Product NDC | 55700-221 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Promethazine Hydrochloride |
Non-Proprietary Name | Promethazine Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20140709 |
Marketing Category Name | ANDA |
Application Number | ANDA040712 |
Manufacturer | Quality Care Products LLC |
Substance Name | PROMETHAZINE HYDROCHLORIDE |
Strength | 25 |
Strength Unit | mg/1 |
Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |