| NDC Code | 0615-1547-39 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-1547-39) |
|---|
| Product NDC | 0615-1547 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Chlorpromazine |
|---|
| Non-Proprietary Name | Chlorpromazine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19730103 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA080439 |
|---|
| Manufacturer | NCS HealthCare of KY, Inc dba Vangard Labs |
|---|
| Substance Name | CHLORPROMAZINE HYDROCHLORIDE |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Phenothiazines [CS],Phenothiazine [EPC] |
|---|