43353-772 : Gemfibrozil 600 mg Oral Tablet
NDC: | 43353-772 |
Labeler: | Aphena Pharma Solutions - Tennessee, Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Gemfibrozil |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA078012 |
Rev. Date: |
Appearance:
Markings: | B260 |
Shapes: |
Oval |
Colors: |
White |
Size (mm): | 20 |
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:
- 43353-772-60: 90 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (43353‑772‑60)
Active Ingredients:
- Gemfibrozil
Dosage Strength:
- 600 mg
Inactive Ingredients:
- Calcium Stearate
- Carnauba Wax
- Colloidal Silicon Dioxide
- Croscarmellose Sodium
- Hydroxypropyl Cellulose
- Cellulose, Microcrystalline
- Polyethylene Glycol 3350
- Polyvinyl Alcohol
- Starch, Pregelatinized Corn
- Sodium Lauryl Sulfate
- Talc
- Titanium Dioxide
Pharmaceutical Classes:
- Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]
- PPAR alpha [CS]
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
Related Products:
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- 0591-0454 Gemfibrozil 600 mg Oral Tablet by Watson Laboratories, Inc.
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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.