Phenobarbital
- Product NDC
- 0143-1450
- 11-digit product format
- 001431450
- Labeler code
- 0143
- Product ID
- 0143-1450_8b0f0d64-752d-4827-8455-e3b3c90ff849
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenobarbital
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-03-05
- Marketing end
- 2021-05-31
- Substance
- PHENOBARBITAL
- Active strength
- 30 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0143-1450-01 | 00143145001 | 100 TABLET in 1 BOTTLE (0143-1450-01) | 100 tablet | 2020-03-05 | 2021-05-31 | No | No | Current |
| 0143-1450-05 | 00143145005 | 500 TABLET in 1 BOTTLE (0143-1450-05) | 500 tablet | 2020-03-05 | 2021-05-31 | No | No | Current |