| NDC Code | 58118-0301-6 |
|---|
| Package Description | 60 TABLET, SUGAR COATED in 1 BOTTLE (58118-0301-6) |
|---|
| Product NDC | 58118-0301 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Chlorpromazine Hydrochloride |
|---|
| Non-Proprietary Name | Chlorpromazine Hydrochloride |
|---|
| Dosage Form | TABLET, SUGAR COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20110803 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA084112 |
|---|
| Manufacturer | Clinical Solutions Wholesale |
|---|
| Substance Name | CHLORPROMAZINE HYDROCHLORIDE |
|---|
| Strength | 25 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
|---|