Phenobarbital
- Product NDC
- 67046-1434
- 11-digit product format
- 670461434
- Labeler code
- 67046
- Product ID
- 67046-1434_38f737f8-385d-f2b6-e063-6394a90ac88d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenobarbital
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Coupler LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2025-07-02
- Substance
- PHENOBARBITAL
- Active strength
- 64.8 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 |
|---|
| 67046-1434-3 | 67046143403 | 30 TABLET in 1 BLISTER PACK (67046-1434-3) | 30 tablet | 2025-07-02 | No | No | Historical |