PHENOBARBITAL
- Product NDC
- 58118-0576
- 11-digit product format
- 581180576
- Labeler code
- 58118
- Product ID
- 58118-0576_4c39ddfc-541b-b671-e063-6394a90a460b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PHENOBARBITAL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Clinical Solutions Wholesale, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2025-03-01
- Substance
- PHENOBARBITAL
- Active strength
- 64.8 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- PHENOBARBITAL
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PHENOBARBITAL | 64.8 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | YQE403BP4D |
| Rxcui | 199167, 199168 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 58118-0576-8 | PHENOBARBITAL | 30 in 1 BLISTER PACK | TABLET | 30 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 58118-0576-8 | 58118057608 | 30 TABLET in 1 BLISTER PACK (58118-0576-8) | 30 tablet | 2026-03-04 | No | No | Current |