Phenobarbital
- Product NDC
- 69367-438
- 11-digit product format
- 693670438
- Labeler code
- 69367
- Product ID
- 69367-438_e9ead134-956a-408a-8546-3ab0e88229a9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenobarbital
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Westminster Pharmaceuticals, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2026-03-06
- Substance
- PHENOBARBITAL
- Active strength
- 15 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Phenobarbital
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PHENOBARBITAL | 15 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | YQE403BP4D |
| Rxcui | 198083, 198086, 198089, 199164, 199167, 199168, 312357, 312362 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69367-438-01 | Phenobarbital | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
| 69367-438-05 | Phenobarbital | 500 in 1 BOTTLE | TABLET | 500 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 69367-438-01 | 69367043801 | 100 TABLET in 1 BOTTLE (69367-438-01) | 100 tablet | 2026-03-06 | No | No | Current |
| 69367-438-05 | 69367043805 | 500 TABLET in 1 BOTTLE (69367-438-05) | 500 tablet | 2026-03-06 | No | No | Current |