Phenobarbital
- Product NDC
- 72162-1582
- 11-digit product format
- 721621582
- Labeler code
- 72162
- Product ID
- 72162-1582_0e6eb3a1-f9ab-453f-ace9-d7fa4a1464c5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- phenobarbital
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-03-01
- Substance
- PHENOBARBITAL
- Active strength
- 30 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 |
|---|
| 72162-1582-1 | 72162158201 | 100 TABLET in 1 BOTTLE, PLASTIC (72162-1582-1) | 100 tablet | 2023-04-21 | No | No | Historical |
| 72162-1582-5 | 72162158205 | 500 TABLET in 1 BOTTLE, PLASTIC (72162-1582-5) | 500 tablet | 2023-04-21 | No | No | Historical |