Phenobarbital
- Product NDC
- 72162-1267
- 11-digit product format
- 721621267
- Labeler code
- 72162
- Product ID
- 72162-1267_7c1c85c9-6581-42f8-8e33-2cc4722934a7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenobarbital
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-11-01
- Substance
- PHENOBARBITAL
- Active strength
- 16.2 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 | 16.2 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | YQE403BP4D |
| Rxcui | 198086 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1267-0 | Phenobarbital | 1000 in 1 BOTTLE | TABLET | 1000 | | 102 |
| 72162-1267-1 | Phenobarbital | 100 in 1 BOTTLE | TABLET | 100 | | 102 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1267 | PHENOBARBITAL TABLET [BRYANT RANCH PREPACK] | 102 | Current NDC, 2 package rows | 20240329_2c238b77-6806-44af-9a66-fd871eaddfc0.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 |
|---|
| 72162-1267-0 | 72162126700 | 1000 TABLET in 1 BOTTLE (72162-1267-0) | 1000 tablet | 2023-10-06 | No | No | Historical |
| 72162-1267-1 | 72162126701 | 100 TABLET in 1 BOTTLE (72162-1267-1) | 100 tablet | 2023-10-06 | No | No | Historical |