Baclofen
- Product NDC
- 55700-408
- 11-digit product format
- 557000408
- Labeler code
- 55700
- Product ID
- 55700-408_eeddb575-26b6-472e-a31d-983ca704bc18
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- baclofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA077241
- Marketing category
- ANDA
- Marketing start
- 2005-12-01
- 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
- 2023-12-31
- 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 |
|---|
| 55700-408-01 | 55700040801 | 120 TABLET in 1 BOTTLE, PLASTIC (55700-408-01) | 120 tablet | 2016-04-28 | 0000-00-00 | No | No | Current |
| 55700-408-30 | 55700040830 | 30 TABLET in 1 BOTTLE, PLASTIC (55700-408-30) | 30 tablet | 2016-04-28 | 0000-00-00 | No | No | Current |
| 55700-408-60 | 55700040860 | 60 TABLET in 1 BOTTLE, PLASTIC (55700-408-60) | 60 tablet | 2016-04-28 | 0000-00-00 | No | No | Current |
| 55700-408-90 | 55700040890 | 90 TABLET in 1 BOTTLE, PLASTIC (55700-408-90) | 90 tablet | 2016-04-28 | 0000-00-00 | No | No | Current |