| NDC Code | 16571-136-50 |
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| Package Description | 500 TABLET in 1 BOTTLE (16571-136-50) |
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| Product NDC | 16571-136 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Atorvastatin Calcium |
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| Non-Proprietary Name | Atorvastatin Calcium, Film Coated |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20231020 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA209912 |
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| Manufacturer | Rising Pharma Holdings, Inc. |
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| Substance Name | ATORVASTATIN CALCIUM TRIHYDRATE |
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| Strength | 10 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
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