NDC 50090-4682-01 - Baclofen
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 50090-4682
- Requested NDC
- 50090-4682-01
- Package NDCs from labels
- 50090-4682-0, 50090-4682-1, 50090-4682-2, 50090-4682-3, 50090-4682-01
- Manufacturer
- A-S Medication Solutions
- Effective date
- 2026-01-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Baclofen - A-S Medication Solutions | A-S Medication Solutions | 2026-01-20 | HUMAN PRESCRIPTION DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 50090-4682-0 | 2023-02-07 | BACLOFEN TABLETS USP Rx only |
| 50090-4682-1 | 2023-02-07 | BACLOFEN TABLETS USP Rx only |
| 50090-4682-2 | 2023-02-07 | BACLOFEN TABLETS USP Rx only |
| 50090-4682-3 | 2023-02-07 | BACLOFEN TABLETS USP Rx only |
| 50090-4682-0 | 2023-01-30 | BACLOFEN TABLETS USP Rx only |
| 50090-4682-1 | 2023-01-30 | BACLOFEN TABLETS USP Rx only |
| 50090-4682-2 | 2023-01-30 | BACLOFEN TABLETS USP Rx only |
| 50090-4682-3 | 2023-01-30 | BACLOFEN TABLETS USP Rx only |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50090-4682-0 | Baclofen | 20 in 1 BOTTLE | TABLET | 20 | 12 | |
| 50090-4682-1 | Baclofen | 60 in 1 BOTTLE | TABLET | 60 | 12 | |
| 50090-4682-2 | Baclofen | 30 in 1 BOTTLE | TABLET | 30 | 12 | |
| 50090-4682-3 | Baclofen | 90 in 1 BOTTLE | TABLET | 90 | 12 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50090-4682 | BACLOFEN TABLET [A-S MEDICATION SOLUTIONS] | 10 | Current NDC, Legacy NDC, 4 package rows | 20240430_975fda6d-d929-482b-8be7-60849026dbdd.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50090-4682-1 | EA - Each | 50090-4682 | a8fc15fc-6d4b-4788-ba03-566e76bdfed0 | 1 | 2024-02-14 |
| 50090-4682-2 | EA - Each | 50090-4682 | 3eb7237c-6305-44d3-b5e3-74c0e2f28cf3 | 1 | 2024-02-14 |
| 50090-4682-3 | EA - Each | 50090-4682 | 8d51c202-45e2-4b14-8427-b07835e7953a | 1 | 2024-02-14 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Lactation Flow Drops 2149 | LACTATION FLOW DROPS | Professional Complementary Health Formulas | 66a063c4-aa38-4c8e-b361-ee841165edeb | 2026-01-08 | Warnings | L11K75P92J |
| Nocturnal Enuresis Drops 2011 | NOCTURNAL ENURESIS DROPS | Professional Complementary Health Formulas | 9cd29086-c9eb-4db1-a219-2a8bae3663d8 | 2026-01-08 | Warnings | L11K75P92J |
| Ledum Combination 9257 | LEDUM COMBINATION | Professional Complementary Health Formulas | 38b89b32-4915-487d-8b2d-250123487b15 | 2026-01-08 | Warnings | L11K75P92J |
| RET Lung 7003 | RET LUNG | Professional Complementary Health Formulas | 2ed03832-f226-4b3c-9ee6-5352f8d79fdb | 2026-01-08 | Warnings | L11K75P92J |
| Myosotis Combination 9234 | MYOSOTIS COMBINATION | Professional Complementary Health Formulas | 8cc292dc-b959-4d81-8277-03044992fccb | 2026-01-08 | Warnings | L11K75P92J |
| Anti-Scar Drops 2084 | ANTI-SCAR DROPS | Professional Complementary Health Formulas | ad0e9159-ed68-48aa-a7d1-7ff5c32ec304 | 2026-01-08 | Warnings | L11K75P92J |
| Fifth Chakra (Throat) 7305 | FIFTH CHAKRA (THROAT) | Professional Complementary Health Formulas | b731f708-10a8-451f-8550-1e7302102b96 | 2026-01-08 | Warnings | L11K75P92J |
| Dementia Drops 2117 | DEMENTIA DROPS | Professional Complementary Health Formulas | 83aec02b-bc62-49a2-ba35-4ac94f9bfc6e | 2026-01-08 | Warnings | L11K75P92J |
| Baclofen | BACLOFEN | Palmetto Pharmaceuticals Inc. | 2422746c-afec-ad30-e063-6394a90a0403 | 2025-12-31 | Warnings, Adverse reactions | H789N3FKE8 |
| Medicated Cornstarch Baby Powder | ACTIVE CORN STARCH | Davion, Inc. | e39032d1-c8cd-4a41-af10-126970b8ad38 | 2025-12-29 | Warnings | O8232NY3SJ |
| Baclofen | BACLOFEN | Northwind Health Company, LLC | 06bcfb08-2ada-f803-e063-6394a90a826b | 2025-12-26 | Warnings, Adverse reactions | 197391 H789N3FKE8 |
| BACLOFEN | BACLOFEN | Advanced Rx of Tennessee, LLC | 459ec5f5-4f99-e917-e063-6294a90a23cd | 2025-12-18 | Warnings, Adverse reactions | 197391 H789N3FKE8 |
| Baclofen | BACLOFEN | Wilshire Pharmaceuticals, Inc. | 4585aafe-0af8-4786-a419-6a7e76671ca2 | 2025-12-16 | Warnings, Adverse reactions | H789N3FKE8 |
| FLEQSUVY | BACLOFEN | Azurity Pharmaceuticals, Inc. | 9076d6ce-bbc2-4a9f-9cb9-2de1b675b9aa | 2025-12-16 | Warnings, Adverse reactions | H789N3FKE8 |
| Baclofen | BACLOFEN | PHOENIX RX LLC | 45c6d45d-95d5-21b8-e063-6294a90a7955 | 2025-12-12 | Warnings, Adverse reactions | 197392 H789N3FKE8 |
| Baclofen | BACLOFEN | Upsher-Smith Laboratories, LLC | b2747a9d-5fca-4657-9e4b-4112607f30d8 | 2025-12-11 | Warnings, Adverse reactions | 197391 197392 H789N3FKE8 |
| BACLOFEN | BACLOFEN | Advagen Pharma Limited | d63af5f0-c275-480b-89b5-6cf1ad55ab63 | 2025-12-09 | Boxed warning, Warnings, Adverse reactions | H789N3FKE8 |
| BACLOFEN | BACLOFEN | SOLA Pharmaceuticals, LLC | 7b308b35-8c08-458d-860e-c78d057e8260 | 2025-12-08 | Warnings, Adverse reactions | 197391 H789N3FKE8 |
| Baclofen | BACLOFEN | ANI Pharmaceuticals, Inc. | c73ed3af-8e8a-4a18-90fc-a0f2dcc641d0 | 2025-12-04 | Warnings, Adverse reactions | H789N3FKE8 |
| BACLOFEN | BACLOFEN | Proficient Rx LP | 0680301a-1649-46c4-b74e-ab03967945d0 | 2025-12-01 | Warnings, Adverse reactions | 197391 H789N3FKE8 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.