NDC 21695-014-30 - 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
- 21695-014
- Requested NDC
- 21695-014-30
- Package NDCs from labels
- 21695-014-30, 21695-014-42, 21695-014-60, 21695-014-90, 21695-014-72
- Manufacturer
- Rebel Distributors Corp.
- Effective date
- 2009-12-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Baclofen Tablets USP 10mg & 20mg | Rebel Distributors Corp. | 2009-12-01 | HUMAN PRESCRIPTION DRUG LABEL |
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2012-07-24 | Indexing - Billing Unit |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 21695-014-42 | 2019-09-24 | C162847 | 48780-1 | 934fe258-4c6e-48b1-e053-8cdaa90a720a | Baclofen Tablets USP 10mg & 20mg |
| 21695-014-72 | 2019-09-24 | C162847 | 48780-1 | 934fe258-4c6e-48b1-e053-8cdaa90a720a | Baclofen Tablets USP 10mg & 20mg |
| 21695-014-90 | 2019-09-24 | C162847 | 48780-1 | 934fe258-4c6e-48b1-e053-8cdaa90a720a | Baclofen Tablets USP 10mg & 20mg |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 21695-014-30 | Baclofen | 30 in 1 BOTTLE | TABLET | 30 | 1 | |
| 21695-014-42 | Baclofen | 42 in 1 BOTTLE | TABLET | 42 | 1 | |
| 21695-014-60 | Baclofen | 60 in 1 BOTTLE | TABLET | 60 | 1 | |
| 21695-014-72 | Baclofen | 120 in 1 BOTTLE | TABLET | 120 | 1 | |
| 21695-014-90 | Baclofen | 90 in 1 BOTTLE | TABLET | 90 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 21695-014-30 | EA - Each | 21695-014 | 045b5479-8a48-4d8c-9230-f5d2a183b569 | 1 | 2012-07-24 |
| 21695-014-60 | EA - Each | 21695-014 | f974850f-d5fd-43d0-8ba4-4c7e7a277577 | 1 | 2012-07-24 |
| 21695-014-72 | EA - Each | 21695-014 | 67d2f2c6-d0bc-41c7-872b-eb0966b54255 | 1 | 2012-07-24 |
| 21695-014-90 | EA - Each | 21695-014 | 10ba6395-b45c-47ec-8f19-96e039588df3 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| BACLOFEN | ACTIVE INGREDIENT | H789N3FKE8 | BACLOFEN TABLET [REBEL DISTRIBUTORS CORP.] | 1 | |
| BACLOFEN | ACTIVE MOIETY | H789N3FKE8 | BACLOFEN TABLET [REBEL DISTRIBUTORS CORP.] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | BACLOFEN TABLET [REBEL DISTRIBUTORS CORP.] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | BACLOFEN TABLET [REBEL DISTRIBUTORS CORP.] | 1 | |
| POVIDONE | INACTIVE INGREDIENT | FZ989GH94E | BACLOFEN TABLET [REBEL DISTRIBUTORS CORP.] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | BACLOFEN TABLET [REBEL DISTRIBUTORS CORP.] | 1 |
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 |
|---|---|---|---|---|---|---|
| BACLOFEN | BACLOFEN | REMEDYREPACK INC. | ab3760cd-a84b-49ba-88e3-b9ea73c55f82 | 2026-09-09 | Warnings, Adverse reactions | 197391 H789N3FKE8 |
| Leader Artificial Tears 15 mL | POLYVINYL ALCOHOL, POVIDONE | Cardinal Health | 8cccc589-3a8e-baad-e053-2a95a90ab8c7 | 2026-09-09 | Warnings | FZ989GH94E |
| Baclofen | BACLOFEN | Atlantic Biologicals Corp. | 50b3e7be-832b-313d-e063-6394a90a5ab4 | 2026-09-04 | Warnings, Adverse reactions | H789N3FKE8 |
| FRESHKOTE PRESERVATIVE FREE LUBRICANT EYE DROPS | POVIDONE, POLYVINYL ALCOHOL SOLUTION | Harrow Eye, LLC | 049e9cc9-0663-53bc-e063-6294a90a2c4f | 2026-09-04 | Warnings | FZ989GH94E |
| BACLOFEN | BACLOFEN | REMEDYREPACK INC. | 4e2cd27d-91c7-4f15-96cc-3971769dbeaa | 2026-09-03 | Warnings, Adverse reactions | 197392 H789N3FKE8 |
| BACLOFEN | BACLOFEN | REMEDYREPACK INC. | c2e1d183-7061-459b-a631-206b06d12753 | 2026-09-01 | Warnings, Adverse reactions | 197392 H789N3FKE8 |
| Baclofen | BACLOFEN | Par Health USA, LLC | c17527be-661d-42f5-b6f6-56a681ba7870 | 2026-08-24 | Warnings, Adverse reactions | 197391 197392 H789N3FKE8 |
| Baclofen | BACLOFEN | Bryant Ranch Prepack | aeb56b0e-7126-4417-b726-e8a54f73de3f | 2026-08-24 | Warnings, Adverse reactions | 197392 H789N3FKE8 |
| Rohto Optic Glow | NAPHAZOLINE HYDROCHLORIDE, POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | df9c5f7c-96e6-4b2b-b8cb-21a6a3342dff | 2026-08-20 | Warnings | FZ989GH94E |
| Rohto Preservative Free Dry Aid | POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | f4b1974c-2412-45f6-b79d-88b8a0bcb608 | 2026-08-18 | Warnings | FZ989GH94E |
| Rohto Dry-Aid | POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | 8ea5c6c9-48f4-406a-a2cb-9280c546d87d | 2026-08-18 | Warnings | FZ989GH94E |
| BACLOFEN | BACLOFEN | REMEDYREPACK INC. | ac9b720f-b755-49f1-9850-efb26feadaeb | 2026-08-14 | Warnings, Adverse reactions | 197391 H789N3FKE8 |
| BACLOFEN | BACLOFEN | REMEDYREPACK INC. | 355266e4-68f7-47d7-9f4e-1a0fc912786d | 2026-08-10 | Warnings, Adverse reactions | 197392 H789N3FKE8 |
| Baclofen | BACLOFEN | REMEDYREPACK INC. | 76896b07-2835-4467-b386-87ec66ddd88e | 2026-08-04 | Warnings, Adverse reactions | 197391 H789N3FKE8 |
| Baclofen | BACLOFEN | Cardinal Health 107, LLC | 3c87e116-871d-46b8-897b-fc27a17b988d | 2026-07-24 | Warnings, Adverse reactions | H789N3FKE8 |
| Baclofen | BACLOFEN | Preferred Pharmaceuticals Inc. | 3047613d-006b-4011-b5fe-098588f474aa | 2026-07-22 | Warnings, Adverse reactions | 197392 H789N3FKE8 |
| GOOD NEIGHBOR PHARMACY ARTIFICAL TEARS LUBRICANT EYE DROPS | POLYVINYL ALCOHOL, POVIDONE | AmerisourceBergen | ce6852a8-c5e6-403d-a7b4-a2e85d1ebb1f | 2026-07-22 | Warnings | FZ989GH94E |
| Baclofen | BACLOFEN | REMEDYREPACK INC. | 6274e70a-fb57-461b-b1bc-39d4ff916b2a | 2026-07-14 | Warnings, Adverse reactions | 197392 H789N3FKE8 |
| Baclofen | BACLOFEN | REMEDYREPACK INC. | ebbfec9e-621c-4d04-8a1c-81d2eb9e9c74 | 2026-06-30 | Warnings, Adverse reactions | 197392 H789N3FKE8 |
| Baclofen | BACLOFEN | AvPAK | c21095a9-17b1-555a-e053-2a95a90a51fd | 2026-06-29 | Warnings, Adverse reactions | H789N3FKE8 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.