| NDC Code | 23155-068-10 |
|---|
| Package Description | 1000 TABLET in 1 BOTTLE (23155-068-10) |
|---|
| Product NDC | 23155-068 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Promethazine Hydrochloride |
|---|
| Non-Proprietary Name | Promethazine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20130217 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040673 |
|---|
| Manufacturer | Heritage Pharmaceuticals Inc. |
|---|
| Substance Name | PROMETHAZINE HYDROCHLORIDE |
|---|
| Strength | 25 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Phenothiazine [EPC],Phenothiazines [CS] |
|---|