Phenobarbital
- Product NDC
- 69367-628
- 11-digit product format
- 693670628
- Labeler code
- 69367
- Product ID
- 69367-628_d27572eb-a595-4050-a278-6a219541ad67
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenobarbital
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Westminster Pharmaceuticals, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2023-09-08
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Phenobarbital
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PHENOBARBITAL | 97.2 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | YQE403BP4D |
| Rxcui | 198086, 199164, 199167, 199168 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69367-628-01 | Phenobarbital | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
| 69367-628-10 | Phenobarbital | 1000 in 1 BOTTLE | TABLET | 1000 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69367-628 | PHENOBARBITAL TABLET [WESTMINSTER PHARMACEUTICALS, LLC] | 1 | Current NDC, 2 package rows | 20230915_f8ba853a-d699-4a91-a23d-9ac9b9dbe69a.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 |
|---|
| 69367-628-01 | 69367062801 | 100 TABLET in 1 BOTTLE (69367-628-01) | 100 tablet | 2023-09-08 | No | No | Current |
| 69367-628-10 | 69367062810 | 1000 TABLET in 1 BOTTLE (69367-628-10) | 1000 tablet | 2023-09-08 | No | No | Current |