| NDC Code | 70934-243-10 |
|---|
| Package Description | 10 TABLET in 1 BOTTLE, PLASTIC (70934-243-10) |
|---|
| Product NDC | 70934-243 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Promethazine Hydrochloride |
|---|
| Non-Proprietary Name | Promethazine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20190204 |
|---|
| End Marketing Date | 20230930 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040712 |
|---|
| Manufacturer | Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
|---|
| Substance Name | PROMETHAZINE HYDROCHLORIDE |
|---|
| Strength | 25 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |
|---|