Phenobarbital
- Product NDC
- 70518-4129
- 11-digit product format
- 705184129
- Labeler code
- 70518
- Product ID
- 70518-4129_3fa56bec-cf88-ce76-e063-6294a90ae2bb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenobarbital
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2024-07-01
- Substance
- PHENOBARBITAL
- Active strength
- 32.4 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 | 32.4 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | YQE403BP4D |
| Rxcui | 199167 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4129-0 | Phenobarbital | 30 in 1 BLISTER PACK | TABLET | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-4129 | PHENOBARBITAL TABLET [REMEDYREPACK INC.] | 2 | Current NDC, 1 package rows | 20250424_4e2910f2-173d-4b5c-aad3-44f4ab40d8cb.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 |
|---|
| 70518-4129-0 | 70518412900 | 30 TABLET in 1 BLISTER PACK (70518-4129-0) | 30 tablet | 2024-07-01 | No | No | Historical |