| NDC Code | 47335-539-08 |
|---|
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-539-08) |
|---|
| Product NDC | 47335-539 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Niacin |
|---|
| Non-Proprietary Name | Niacin |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20140627 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA200484 |
|---|
| Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|
| Substance Name | NIACIN |
|---|
| Strength | 500 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Nicotinic Acid [EPC], Nicotinic Acids [CS] |
|---|