Antabuse
- Product NDC
- 51285-524
- 11-digit product format
- 512850524
- Labeler code
- 51285
- Product ID
- 51285-524_f94e573e-5f61-47c9-8e9c-be1ce5aa49ce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Disulfiram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Teva Women's Health, Inc.
- Application
- ANDA088483
- Marketing category
- ANDA
- Marketing start
- 2006-02-01
- Marketing end
- 2021-09-30
- Substance
- DISULFIRAM
- Active strength
- 500 mg/1
- Pharmacologic classes
- Acetyl Aldehyde Dehydrogenase Inhibitors [MoA],Aldehyde Dehydrogenase Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51285-524-02 | 51285052402 | 100 TABLET in 1 BOTTLE (51285-524-02) | 100 tablet | 2006-02-01 | 2021-09-30 | No | No | Current |