NDC 51672-2130-01 - IBUPROFEN
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
- 51672-2130
- Requested NDC
- 51672-2130-01
- Package NDCs from labels
- 51672-2130-8, 51672-2130-1, 51672-2130-01
- Manufacturer
- HF Acquisition Co LLC, DBA HealthFirst
- Effective date
- 2026-07-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| IBUPROFEN - HF Acquisition Co LLC, DBA HealthFirst | HF Acquisition Co LLC, DBA HealthFirst | 2026-07-23 | HUMAN OTC DRUG LABEL |
| Ibuprofen | Preferred Pharmaceuticals Inc. | 2026-03-25 | HUMAN OTC DRUG LABEL |
| Ibuprofen | Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | 2025-07-07 | HUMAN OTC DRUG LABEL |
| Ibuprofen - A-S Medication Solutions | A-S Medication Solutions | 2024-10-14 | HUMAN OTC DRUG LABEL |
| Ibuprofen - Proficient Rx LP | Proficient Rx LP | 2022-07-01 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-2130-1 | Ibuprofen | 1 in 1 CARTON | SUSPENSION | 1 | 9 | |
| 51672-2130-1 | Ibuprofen | 240 mL in 1 BOTTLE | SUSPENSION | 240 | 9 | |
| 51672-2130-8 | Ibuprofen | 1 in 1 CARTON | SUSPENSION | 1 | 9 | |
| 51672-2130-8 | Ibuprofen | 120 mL in 1 BOTTLE | SUSPENSION | 120 | 9 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-2130 | IBUPROFEN SUSPENSION [SUN PHARMACEUTICAL INDUSTRIES, INC.] | 8 | Current NDC, Legacy NDC, 4 package rows | 20250406_f4dad3d6-1366-4bdf-99eb-370ab74a6b9e.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-2130-1 | ML - Milliliter | 51672-2130 | ec8e73b1-094d-4ee4-9486-99c6adcfc941 | 1 | 2017-12-14 |
| 51672-2130-8 | ML - Milliliter | 51672-2130 | 60e98840-aa05-4a38-8349-ef81b0bc4a3c | 1 | 2017-12-14 |
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 |
|---|---|---|---|---|---|---|
| Fendall 1000 Pure Flow | PURIFIED WATER | Protective Industrial Products, Inc. | 55a2f4da-bb1e-8ead-e063-6394a90af72e | 2026-07-02 | Warnings | 059QF0KO0R |
| Sterile Eyesaline Eyewash | STERILE EYESALINE EYEWASH | Protective Industrial Products, Inc. | 55a290e8-8310-8be4-e063-6394a90abdce | 2026-07-02 | Warnings | 059QF0KO0R |
| Eyesaline Emergency Eyewash | PURIFIED WATER | Protective Industrial Products, Inc. | 55a261c2-725d-6765-e063-6294a90a3260 | 2026-07-02 | Warnings | 059QF0KO0R |
| Remodulin | TREPROSTINIL | United Therapeutics Corporation | 6c80bb38-e8db-4138-9f0d-dbbf9c673185 | 2026-07-02 | Warnings, Adverse reactions | 059QF0KO0R |
| Ibuprofen | IBUPROFEN | Proficient Rx LP | 34a9b94f-93ba-4a7c-92eb-d0b4b530d887 | 2026-07-02 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Dr. Reddy's Laboratories Inc. | 4d830b9b-b396-9581-7572-c7f19ff17597 | 2026-07-01 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | St. Mary's Medical Park Pharmacy | 88dd304f-1c64-08e3-e053-2a95a90a596f | 2026-07-01 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| IBUPROFEN | IBUPROFEN | Amazon.com Services LLC | faabb11a-6fa0-492d-85cc-74ff8175b0b3 | 2026-07-01 | Warnings | WK2XYI10QM |
| Infants Motrin | IBUPROFEN | Kenvue Brands LLC | c2302bfe-b367-4867-b803-29f066a42dc7 | 2026-06-30 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | REMEDYREPACK INC. | 1e6f3ce7-e8a3-40e8-8437-523ef5277b2e | 2026-06-30 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | HAWAII REPACK, INC. | 6239818c-747d-4cbb-9b41-27ca8bbce41b | 2026-06-26 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Sportpharm LLC | cef04ae4-e78a-454d-bb66-84b1d348c106 | 2026-06-26 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Glycerin | GLYCERIN | Beijing Jingfeng Pharmaceutical (Shandong) Co., Ltd | 552d9018-cc7d-7e1a-e063-6294a90a3322 | 2026-06-26 | Warnings | PDC6A3C0OX |
| Ibuprofen mini dye free | IBUPROFEN | CHAIN DRUG MARKETING ASSOCIATION INC. | 552d9018-cc7e-7e1a-e063-6294a90a3322 | 2026-06-26 | Warnings | WK2XYI10QM |
| Glycerin | GLYCERIN | Beijing Jingfeng Pharmaceutical (Shandong) Co., Ltd | 552e16b9-f46a-7838-e063-6394a90ab8aa | 2026-06-26 | Warnings | PDC6A3C0OX |
| Ibuprofen | IBUPROFEN | TOP CARE (Topco Associates LLC) | fb842f4d-1228-9a52-e053-6294a90adb41 | 2026-06-26 | Warnings | WK2XYI10QM |
| ibuprofen | IBUPROFEN | Unit Dose Solutions, Inc. | 551535ce-eab0-bb13-e063-6294a90a2070 | 2026-06-25 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Unit Dose Solutions, Inc. | 5515661b-6373-2191-e063-6294a90a17e0 | 2026-06-25 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Unit Dose Solutions, Inc. | 5515e80f-7513-b425-e063-6294a90aa542 | 2026-06-25 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen Mini Dye Free | IBUPROFEN | CVS Pharmacy | 42c7dbec-2e53-70ae-e063-6294a90a16e6 | 2026-06-25 | Warnings | WK2XYI10QM |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.