51285-523 : Antabuse 250 mg Oral Tablet
NDC: | 51285-523 |
Labeler: | Teva Women's Health, Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Antabuse |
Dosage Form: | Oral Tablet |
Application #: | ANDA088482 |
Rev. Date: |
Appearance:
Markings: | OP;706 |
Shapes: |
Round |
Colors: |
White |
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. |
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:
- 51285-523-02: 100 TABLET IN 1 BOTTLE (51285‑523‑02)
Active Ingredients:
- Disulfiram
Dosage Strength:
- 250 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.- 51285-524 Antabuse 500 mg Oral Tablet by Teva Women's Health, Inc.
- 54868-5034 Antabuse 250 mg Oral Tablet by Physicians Total Care, Inc.
NDC QR Code
Scan the QR code below to easily reference this data in the future:< Prev: 51285-446Next: 51285-524 >
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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.