| NDC Code | 68462-862-01 |
|---|
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (68462-862-01) |
|---|
| Product NDC | 68462-862 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Chlorpromazine Hydrochloride |
|---|
| Non-Proprietary Name | Chlorpromazine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20210323 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA212144 |
|---|
| Manufacturer | Glenmark Pharmaceuticals Inc., USA |
|---|
| Substance Name | CHLORPROMAZINE HYDROCHLORIDE |
|---|
| Strength | 25 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |
|---|