Baclofen
- Product NDC
- 72162-2448
- 11-digit product format
- 721622448
- Labeler code
- 72162
- Product ID
- 72162-2448_f2b53840-4020-4ed6-9c57-87c3a94be4c4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Baclofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212067
- Marketing category
- ANDA
- Marketing start
- 2023-06-15
- Substance
- BACLOFEN
- Active strength
- 5 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Baclofen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BACLOFEN | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | H789N3FKE8 |
| Rxcui | 430902 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2448-1 | Baclofen | 100 in 1 BOTTLE | TABLET | 100 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2448 | BACLOFEN TABLET [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20250124_9bbcbf20-57ed-447b-9744-a5f10b9a057a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2448-1 | 72162244801 | 100 TABLET in 1 BOTTLE (72162-2448-1) | 100 tablet | 2025-01-22 | No | No | Historical |