Phenobarbital
- Product NDC
- 69336-116
- 11-digit product format
- 693360116
- Labeler code
- 69336
- Product ID
- 69336-116_bedf25f2-a330-4069-e053-2995a90acffc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenobarbital
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sterling-Knight Pharmaceuticals, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2017-03-28
- Marketing end
- 0000-00-00
- Substance
- PHENOBARBITAL
- Active strength
- 32 mg/1
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69336-116-10 | 69336011610 | 100 TABLET in 1 PACKAGE (69336-116-10) | 100 tablet | 2017-03-28 | 0000-00-00 | No | No | Current |
| 69336-116-11 | 69336011611 | 1000 TABLET in 1 PACKAGE (69336-116-11) | 1000 tablet | 2017-03-28 | 0000-00-00 | No | No | Current |