Baclofen
- Product NDC
- 70518-0411
- 11-digit product format
- 705180411
- Labeler code
- 70518
- Product ID
- 70518-0411_a47822dc-af86-7c9f-e053-2995a90a0f25
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Baclofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA072235
- Marketing category
- ANDA
- Marketing start
- 2017-04-07
- 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
- 2021-12-31
- 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 |
|---|
| 70518-0411-0 | 70518041100 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-0411-0) | 90 tablet | 2017-04-07 | 0000-00-00 | No | No | Current |
| 70518-0411-1 | 70518041101 | 30 TABLET in 1 BLISTER PACK (70518-0411-1) | 30 tablet | 2017-04-18 | 0000-00-00 | No | No | Current |