Baclofen
- Product NDC
- 50090-5838
- 11-digit product format
- 500905838
- Labeler code
- 50090
- Product ID
- 50090-5838_2f589623-d02a-452a-80b3-b63e44b6746f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Baclofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA212378
- Marketing category
- ANDA
- Marketing start
- 2020-10-14
- Marketing end
- 0000-00-00
- Substance
- BACLOFEN
- Active strength
- 20 mg/1
- Pharmacologic classes
- GABA A Agonists [MoA],GABA B Agonists [MoA],gamma-Aminobutyric Acid-ergic Agonist [EPC]
- 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 |
|---|
| 50090-5838-1 | 50090583801 | 60 TABLET in 1 BOTTLE (50090-5838-1) | 60 tablet | 2021-11-01 | 0000-00-00 | No | No | Current |
| 50090-5838-2 | 50090583802 | 30 TABLET in 1 BOTTLE (50090-5838-2) | 30 tablet | 2021-11-01 | 0000-00-00 | No | No | Current |
| 50090-5838-3 | 50090583803 | 90 TABLET in 1 BOTTLE (50090-5838-3) | 90 tablet | 2021-11-01 | 0000-00-00 | No | No | Current |