Phenobarbital
- Product NDC
- 69367-692
- 11-digit product format
- 693670692
- Labeler code
- 69367
- Product ID
- 69367-692_b8256561-2c8d-4b02-8a59-5fbc524e4eb3
- 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
- 30 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 | 30 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | YQE403BP4D |
| Rxcui | 198083, 198089, 312357, 312362 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69367-692-01 | Phenobarbital | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
| 69367-692-05 | Phenobarbital | 500 in 1 BOTTLE | TABLET | 500 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69367-692 | PHENOBARBITAL TABLET [WESTMINSTER PHARMACEUTICALS, LLC] | 1 | Current NDC, 2 package rows | 20230915_4e70d33b-82f3-4a8e-a35b-ee658b3e0ab1.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 |
|---|
| 69367-692-01 | 69367069201 | 100 TABLET in 1 BOTTLE (69367-692-01) | 100 tablet | 2023-09-08 | No | No | Current |
| 69367-692-05 | 69367069205 | 500 TABLET in 1 BOTTLE (69367-692-05) | 500 tablet | 2023-09-08 | No | No | Current |