51285-524 : Antabuse 500 mg Oral Tablet

Labeler: Teva Women's Health, Inc.
Product Type: Human Prescription Drug
Drug Name:  Antabuse
Dosage Form: Oral Tablet
Application #: ANDA088483
Rev. Date: 


Markings: OP;707
Shapes:  Round
Colors:  White
Size (mm): 13
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.

OP 707: (51285-524) Antabuse 500 mg Oral Tablet by Teva Women's Health, Inc.
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:

  • 51285-524-02: 100 TABLET IN 1 BOTTLE (51285‑524‑02)

Active Ingredients:

  • Disulfiram

Dosage Strength:

  • 500 mg

Inactive Ingredients:

  • Silicon Dioxide
  • Anhydrous Lactose
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Sodium Starch Glycolate Type a Potato
  • Stearic Acid

Pharmaceutical Classes:

  • Acetyl Aldehyde Dehydrogenase Inhibitors [MoA]
  • Aldehyde Dehydrogenase Inhibitor [EPC]

Related Products:

Based on records with the same trade name.
  • 51285-523 Antabuse 250 mg Oral Tablet by Teva Women's Health, Inc.
  • 54868-5034 Antabuse 250 mg Oral Tablet by Physicians Total Care, Inc.


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Note: The MedsChat® 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.