| NDC Code | 47335-539-18 |
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| Package Description | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-539-18) |
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| Product NDC | 47335-539 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Niacin |
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| Non-Proprietary Name | Niacin |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20140627 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA200484 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | NIACIN |
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| Strength | 500 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Nicotinic Acid [EPC], Nicotinic Acids [CS] |
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