69076-611 : Riluzole 50 mg Oral Tablet


NDC: 69076-611
Labeler: Quinn Pharmaceuticals, LLC
Product Type: Human Prescription Drug
Drug Name:  Riluzole
Dosage Form: Oral Tablet
Application #: ANDA204430
Rev. Date: 


Appearance:


Markings: 611
Shapes:  Oval
Colors:  Yellow
Size (mm): 10
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.

NDC Package Codes:

  • 69076-611-60: 60 TABLET IN 1 BOTTLE (69076‑611‑60)

Active Ingredients:

  • Riluzole

Dosage Strength:

  • 50 mg

Inactive Ingredients:

  • Anhydrous Dibasic Calcium Phosphate
  • Silicon Dioxide
  • Croscarmellose Sodium
  • Hypromellose, Unspecified
  • Magnesium Stearate
  • Microcrystalline Cellulose
  • Polyethylene Glycol, Unspecified
  • Titanium Dioxide
  • Ferric Oxide Yellow /

Pharmaceutical Classes:

  • Benzothiazole [EPC]
  • Benzothiazoles [CS]

Related Products:

Based on records with the same trade name.
  • 69076-200 Riluzole 50 mg Oral Tablet, Film Coated by Quinn Pharmaceuticals
  • 0115-3000 Riluzole 50 mg Oral Tablet by Global Pharmaceuticals, Division of Impax Laboratories, Inc.
  • 0179-0150 Riluzole 50 mg Oral Tablet, Film Coated by Kaiser Foundation Hospitals
  • 0179-0217 Riluzole 50 mg Oral Tablet by Kaiser Foundation Hospitals
  • 0378-4145 Riluzole 50 mg Oral Tablet by Mylan Pharmaceuticals Inc.
  • 42291-723 Riluzole 50 mg/1 Oral Tablet, Film Coated by Avkare, Inc.
  • 42291-775 Riluzole 50 mg Oral Tablet, Film Coated by Avkare
  • 60505-3285 Riluzole 50 mg Oral Tablet by Apotex Corp
  • 62756-538 Riluzole 50 mg Oral Tablet by Sun Pharmaceutical Industries Limited
  • 64980-191 Riluzole 50 mg Oral Tablet by Rising Pharmaceuticals, Inc.
  • 67877-286 Riluzole 50 mg Oral Tablet by Ascend Laboratories, LLC
  • 68084-908 Riluzole 50 mg Oral Tablet, Film Coated by American Health Packaging
  • 68462-381 Riluzole 50 mg Oral Tablet by Glenmark Generics Inc., USA

NDC QR Code

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NDC 69076-611 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.