Phenobarbital
- Product NDC
- 13517-693
- 11-digit product format
- 135170693
- Labeler code
- 13517
- Product ID
- 13517-693_8d7c438d-0331-441f-848f-b832658a8728
- 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
- 2026-11-30
- Substance
- PHENOBARBITAL
- Active strength
- 60 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 | 60 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 |
|---|
| 13517-693-01 | Phenobarbital | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 12 |
| 13517-693-05 | Phenobarbital | 500 in 1 BOTTLE, PLASTIC | TABLET | 500 | | 12 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 13517-693 | PHENOBARBITAL TABLET [E5 PHARMA, LLC] | 11 | Current NDC, Legacy NDC, 2 package rows | 20241031_5c4efd5a-75be-480b-ac31-40dd66feada1.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 |
|---|
| 13517-693-01 | 13517069301 | 100 TABLET in 1 BOTTLE, PLASTIC (13517-693-01) | 100 tablet | 2022-11-30 | 2026-11-30 | No | No | Current |
| 13517-693-05 | 13517069305 | 500 TABLET in 1 BOTTLE, PLASTIC (13517-693-05) | 500 tablet | 2022-11-30 | 2026-11-30 | No | No | Current |