Disulfiram
- Product NDC
- 42794-029
- 11-digit product format
- 427940029
- Labeler code
- 42794
- Product ID
- 42794-029_20208d67-134d-2cc1-e063-6394a90a59be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Disulfiram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sigmapharm Laboratories, LLC
- Application
- ANDA091619
- Marketing category
- ANDA
- Marketing start
- 2022-01-11
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Disulfiram
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DISULFIRAM | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | TR3MLJ1UAI |
| Rxcui | 197623, 197624 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42794-029-08 | Disulfiram | 30 in 1 BOTTLE | TABLET | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42794-029 | DISULFIRAM TABLET [SIGMAPHARM LABORATORIES, LLC] | 4 | Current NDC, 1 package rows | 20240821_40f5497f-fe84-43b2-8ff4-32d59edf3917.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 42794-029-08 | 42794002908 | 30 TABLET in 1 BOTTLE (42794-029-08) | 30 tablet | 2022-01-11 | No | No | Current |