70518-1563 : Gemfibrozil 600 mg Oral Tablet
NDC: | 70518-1563 |
Labeler: | Remedyrepack Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Gemfibrozil |
Dosage Form: | Oral Tablet |
Application #: | ANDA077836 |
Rev. Date: |
Appearance:
Markings: | 225;IG |
Shapes: |
Oval |
Colors: |
White |
Size (mm): | 19 |
Segments: * | 2 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces. |
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.
NDC Package Codes:
- 70518-1563-0: 45 TABLET IN 1 BOTTLE, PLASTIC (70518‑1563‑0)
- 70518-1563-1: 30 TABLET IN 1 BLISTER PACK (70518‑1563‑1)
- 70518-1563-2: 90 TABLET IN 1 BOTTLE, PLASTIC (70518‑1563‑2)
- 70518-1563-3: 180 TABLET IN 1 BOTTLE, PLASTIC (70518‑1563‑3)
Active Ingredients:
- Gemfibrozil
Dosage Strength:
- 600 mg
Inactive Ingredients:
- Silicon Dioxide
- Croscarmellose Sodium
- Calcium Stearate
- Microcrystalline Cellulose
- Methylcellulose (15 Mpa.s)
- Hypromellose 2910 (3 Mpa.s)
- Hypromellose 2910 (6 Mpa.s)
- Polyethylene Glycol 400
- Polysorbate 80 /
Pharmaceutical Classes:
- PPAR alpha [CS]
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]
Related Products:
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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.