70518-3977 : Pravastatin Sodium 20 mg Oral Tablet
NDC: | 70518-3977 |
Labeler: | Remedyrepack Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Pravastatin Sodium |
Dosage Form: | Oral Tablet |
Application #: | ANDA077987 |
Rev. Date: |
NDC Package Codes:
- 70518-3977-0: 90 TABLET IN 1 BOTTLE, PLASTIC (70518‑3977‑0)
Active Ingredients:
- Pravastatin Sodium
Dosage Strength:
- 20 mg
Pharmaceutical Classes:
- HMG-CoA Reductase Inhibitor [EPC]
- Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Related Products:
Based on records with the same trade name.- 70518-0304 Pravastatin Sodium 80 mg Oral Tablet by Remedyrepack Inc.
- 70518-0412 Pravastatin Sodium 40 mg Oral Tablet by Remedyrepack Inc.
- 70518-0423 Pravastatin Sodium 20 mg Oral Tablet by Remedyrepack Inc.
- 70518-0549 Pravastatin Sodium 10 mg Oral Tablet by Remedyrepack Inc.
- 70518-0707 Pravastatin Sodium 80 mg Oral Tablet by Remedyrepack Inc.
- 70518-0876 Pravastatin Sodium 40 mg Oral Tablet by Remedyrepack Inc.
- 70518-0936 Pravastatin Sodium 10 mg Oral Tablet by Remedyrepack Inc.
- 70518-0939 Pravastatin Sodium 20 mg Oral Tablet by Remedyrepack Inc.
- 70518-1157 Pravastatin Sodium 10 mg Oral Tablet by Remedyrepack Inc.
- 70518-1197 Pravastatin Sodium 20 mg Oral Tablet by Remedyrepack Inc.
- 70518-1710 Pravastatin Sodium 80 mg Oral Tablet by Remedyrepack Inc.
- 70518-1731 Pravastatin Sodium 20 mg Oral Tablet by Remedyrepack Inc.
- 70518-1862 Pravastatin Sodium 10 mg Oral Tablet by Remedyrepack Inc.
- 70518-1863 Pravastatin Sodium 20 mg Oral Tablet by Remedyrepack Inc.
- 70518-1902 Pravastatin Sodium 40 mg Oral Tablet by Remedyrepack Inc.
- 70518-1938 Pravastatin Sodium 20 mg Oral Tablet by Remedyrepack Inc.
- 70518-2002 Pravastatin Sodium 10 mg Oral Tablet by Remedyrepack Inc.
- 70518-2199 Pravastatin Sodium 80 mg Oral Tablet by Remedyrepack Inc.
- 70518-2229 Pravastatin Sodium 10 mg Oral Tablet by Remedyrepack Inc.
- 70518-2505 Pravastatin Sodium 40 mg Oral Tablet by Remedyrepack Inc.
- More related products ...
NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.