Baclofen
- Product NDC
- 72162-1152
- 11-digit product format
- 721621152
- Labeler code
- 72162
- Product ID
- 72162-1152_e6f4c6ba-3a78-4ae3-8907-ffb525da5057
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Baclofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077156
- Marketing category
- ANDA
- Marketing start
- 2005-08-30
- Substance
- BACLOFEN
- Active strength
- 10 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| H789N3FKE8 | BACLOFEN | 1134-47-0 | BACLOFEN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1152-1 | 72162115201 | 100 TABLET in 1 BOTTLE, PLASTIC (72162-1152-1) | 100 tablet | 2023-08-29 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| BACLOFEN TABLETS, USP | Bryant Ranch Prepack | 2023-08-29 | HUMAN PRESCRIPTION DRUG LABEL | 100 |