Phenobarbital
- Product NDC
- 67046-1543
- 11-digit product format
- 670461543
- Labeler code
- 67046
- Product ID
- 67046-1543_313ea16d-d9b2-654d-e063-6294a90aa6ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenobarbital
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Coupler LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2025-03-26
- Substance
- PHENOBARBITAL
- Active strength
- 97.2 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| YQE403BP4D | PHENOBARBITAL | 50-06-6 | PHENOBARBITAL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67046-1543-3 | 67046154303 | 30 TABLET in 1 BLISTER PACK (67046-1543-3) | 30 tablet | 2025-03-26 | No | No | Historical |