70518-0527 : Linezolid 600 mg Oral Tablet, Film Coated
NDC: | 70518-0527 |
Labeler: | Remedyrepack Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Linezolid |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA204239 |
Rev. Date: |
Appearance:
Markings: | I;22 |
Shapes: |
Oval |
Colors: |
White |
Size (mm): | 18 |
Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. |
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:
- 70518-0527-0: 10 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC (70518‑0527‑0)
Active Ingredients:
- Linezolid
Dosage Strength:
- 600 mg
Inactive Ingredients:
- Silicon Dioxide
- Hypromelloses
- Lactose Monohydrate
- Magnesium Stearate
- Polacrilin Potassium
- Titanium Dioxide
- Polyethylene Glycols
- Carnauba Wax
Pharmaceutical Classes:
- Oxazolidinone Antibacterial [EPC]
- Oxazolidinones [CS]
Related Products:
Based on records with the same trade name.- 70518-4034 Linezolid 600 mg Oral Tablet, Film Coated by Remedyrepack Inc.
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- 43386-022 Linezolid 600 mg Oral Tablet by Lupin Pharmaceuticals, Inc.
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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.