PHENOBARBITAL
- Product NDC
- 64950-574
- 11-digit product format
- 649500574
- Labeler code
- 64950
- Product ID
- 64950-574_ec88f9c0-b075-49a7-acda-8dc7a84b2aee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PHENOBARBITAL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Genus Lifesciences
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2025-03-01
- Substance
- PHENOBARBITAL
- Active strength
- 32.4 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 | 32.4 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | YQE403BP4D |
| Rxcui | 198083, 198086, 198089, 199164, 199167, 199168, 312357, 312362 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 64950-574-01 | PHENOBARBITAL | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
| 64950-574-10 | PHENOBARBITAL | 1000 in 1 BOTTLE | TABLET | 1000 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64950-574 | PHENOBARBITAL TABLET [GENUS LIFESCIENCES] | 1 | Current NDC, 2 package rows | 20250305_074e875d-474a-4bbc-9008-821d63ca9e32.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 |
|---|
| 64950-574-01 | 64950057401 | 100 TABLET in 1 BOTTLE (64950-574-01) | 100 tablet | 2025-03-01 | No | No | Current |
| 64950-574-10 | 64950057410 | 1000 TABLET in 1 BOTTLE (64950-574-10) | 1000 tablet | 2025-03-01 | No | No | Current |