Phenobarbital
- Product NDC
- 13517-625
- 11-digit product format
- 135170625
- Labeler code
- 13517
- Product ID
- 13517-625_326d57e5-b0f8-439f-abd6-186f241e01ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- phenobarbital
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- e5 Pharma, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2022-11-30
- Marketing end
- 2026-09-30
- Substance
- PHENOBARBITAL
- Active strength
- 16.2 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Phenobarbital
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PHENOBARBITAL | 16.2 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 |
|---|
| 13517-625-01 | Phenobarbital | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 13 |
| 13517-625-10 | Phenobarbital | 1000 in 1 BOTTLE, PLASTIC | TABLET | 1000 | | 13 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 13517-625 | PHENOBARBITAL TABLET [E5 PHARMA, LLC] | 12 | Current NDC, Legacy NDC, 2 package rows | 20241031_884f7b62-160a-46c3-92d4-1031b255b76c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 13517-625-01 | 13517062501 | 100 TABLET in 1 BOTTLE, PLASTIC (13517-625-01) | 100 tablet | 2022-11-30 | 2026-06-30 | No | No | Current |
| 13517-625-10 | 13517062510 | 1000 TABLET in 1 BOTTLE, PLASTIC (13517-625-10) | 1000 tablet | 2022-11-30 | 0000-00-00 | No | No | Current |