Disulfiram
- Product NDC
- 0093-5036
- 11-digit product format
- 000935036
- Labeler code
- 0093
- Product ID
- 0093-5036_ae77a576-7b5b-454e-9d2f-b64cc365d6ef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Disulfiram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA088483
- Marketing category
- ANDA
- Marketing start
- 2011-07-19
- 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 |
|---|
| 0093-5036-01 | 00093503601 | 100 TABLET in 1 BOTTLE (0093-5036-01) | 100 tablet | 2011-07-19 | 2021-09-30 | No | No | Current |