BACLOFEN
- Product NDC
- 70512-782
- 11-digit product format
- 705120782
- Labeler code
- 70512
- Product ID
- 70512-782_45723949-ac04-69ef-e063-6294a90a29a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BACLOFEN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- SOLA Pharmaceuticals, LLC
- Application
- ANDA209102
- Marketing category
- ANDA
- Marketing start
- 2025-03-21
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BACLOFEN
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BACLOFEN | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | H789N3FKE8 |
| Rxcui | 197391 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70512-782-10 | BACLOFEN | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70512-782 | BACLOFEN TABLET [SOLA PHARMACEUTICALS, LLC] | 2 | Current NDC, 1 package rows | 20250328_7b308b35-8c08-458d-860e-c78d057e8260.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 |
|---|
| 70512-782-10 | 70512078210 | 100 TABLET in 1 BOTTLE, PLASTIC (70512-782-10) | 100 tablet | 2025-03-21 | No | No | Current |