| NDC Code | 57664-109-88 |
|---|
| Package Description | 100 TABLET in 1 BOTTLE (57664-109-88) |
|---|
| Product NDC | 57664-109 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Promethazine Hydrochloride |
|---|
| Non-Proprietary Name | Promethazine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20090127 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040863 |
|---|
| Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|
| Substance Name | PROMETHAZINE HYDROCHLORIDE |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Phenothiazine [EPC],Phenothiazines [CS] |
|---|