Baclofen
- Product NDC
- 58657-930
- 11-digit product format
- 586570930
- Labeler code
- 58657
- Product ID
- 58657-930_3aa113f3-27d5-328b-e063-6394a90af9e5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Baclofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Method Pharmaceuticals LLC
- Application
- ANDA212378
- Marketing category
- ANDA
- Marketing start
- 2024-06-15
- 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 | 197391, 197392, 430902 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 58657-930-01 | Baclofen | 10 in 1 CARTON | TABLET | 10 | | 2 |
| 58657-930-05 | Baclofen | 5 in 1 CARTON | TABLET | 5 | | 2 |
| 58657-930-10 | Baclofen | 10 in 1 BLISTER PACK | TABLET | 10 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 58657-930-01 | 58657093001 | 10 BLISTER PACK in 1 CARTON (58657-930-01) / 10 TABLET in 1 BLISTER PACK (58657-930-10) | 10 blister pack | 2025-06-01 | No | No | Current |
| 58657-930-05 | 58657093005 | 5 BLISTER PACK in 1 CARTON (58657-930-05) / 10 TABLET in 1 BLISTER PACK (58657-930-10) | 5 blister pack | 2025-06-01 | No | No | Current |
| 58657-930-10 | 58657093010 | 10 in 1 BLISTER PACK | | | | | Historical |