Disulfiram
- Product NDC
- 0093-5035
- 11-digit product format
- 000935035
- Labeler code
- 0093
- Product ID
- 0093-5035_f853e0f6-1b75-4951-a833-cc076ed8e069
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Disulfiram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA088482
- Marketing category
- ANDA
- Marketing start
- 2011-04-15
- Marketing end
- 2021-11-30
- Substance
- DISULFIRAM
- Active strength
- 250 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 |
|---|
| 0093-5035-01 | 00093503501 | 100 TABLET in 1 BOTTLE (0093-5035-01) | 100 tablet | 2011-04-15 | 2021-11-30 | No | No | Current |