| NDC Code | 0832-6019-00 |
|---|
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (0832-6019-00) |
|---|
| Product NDC | 0832-6019 |
|---|
| 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 | 20110803 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA084113 |
|---|
| Manufacturer | Upsher-Smith Laboratories, LLC |
|---|
| Substance Name | CHLORPROMAZINE HYDROCHLORIDE |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |
|---|