Phenobarbital
- Product NDC
- 63629-2042
- 11-digit product format
- 636292042
- Labeler code
- 63629
- Product ID
- 63629-2042_35247cf0-f986-48fb-9a29-a06b4a5513ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- phenobarbital
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-03-01
- Substance
- PHENOBARBITAL
- Active strength
- 15 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 | 15 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | YQE403BP4D |
| Rxcui | 312357 |
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 |
|---|
| 63629-2042-1 | 63629204201 | 500 TABLET in 1 BOTTLE (63629-2042-1) | 500 tablet | 2020-03-01 | 0000-00-00 | No | No | Current |