Phenobarbital
- Product NDC
- 72162-1583
- 11-digit product format
- 721621583
- Labeler code
- 72162
- Product ID
- 72162-1583_0428273f-9cd4-c4fa-e063-6294a90ae594
- 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
- 60 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 | 60 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | YQE403BP4D |
| Rxcui | 198089 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1583-1 | Phenobarbital | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1583 | PHENOBARBITAL TABLET [BRYANT RANCH PREPACK] | 101 | Current NDC, 1 package rows | 20230831_e9c5ca6b-b3b6-46da-9fbe-6f4ed7a33dbb.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 |
|---|
| 72162-1583-1 | 72162158301 | 100 TABLET in 1 BOTTLE, PLASTIC (72162-1583-1) | 100 tablet | 2023-04-21 | No | No | Historical |