Home NDC 70677-0152-01 NDC 70677-0152-01 - Ibuprofen Oral 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 70677-0152
Requested NDC 70677-0152-01
Package NDCs from labels 70677-0152-1, 70677-0152-01
Manufacturer Strategic Sourcing Services | AptaPharma Inc.
Effective date 2022-08-10
Current FDA listing Not matched in FDA.report NDC product tables
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70677-0152-1 Ibuprofen Oral 1 in 1 CARTON SUSPENSION 1 1 70677-0152-1 Ibuprofen Oral 118 mL in 1 BOTTLE SUSPENSION 118 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70677-0152 IBUPROFEN ORAL (IBUPROFEN ORAL) SUSPENSION [STRATEGIC SOURCING SERVICES] 1 Current NDC, Legacy NDC, 2 package rows 20220811_a3062142-db0e-4758-a762-2b2bb05670b1.zip
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.
Matched openFDA labels page 87 of 94 · 1,870 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Circle K Ibuprofen IBUPROFEN Lil Drug Store Products, Inc 805d9d80-7de7-49d9-afdb-3a645059fe35 2022-09-21 Warnings Exact identifier unii: WK2XYI10QM Sterile Water WATER Medical Purchasing Solutions, LLC e90b47e3-9636-b9ee-e053-2a95a90ad48c 2022-09-19 Warnings, Adverse reactions Exact identifier unii: 059QF0KO0R REFRESH OPTIVE Advanced CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, POLYSORBATE 80 Allergan, Inc. ebd0839e-2e1d-4e0e-986c-19f1f5c76358 2022-09-15 Warnings Exact identifier unii: PDC6A3C0OX unii: 6OZP39ZG8H unii: K679OBS311 Ibuprofen IBUPROFEN Aurohealth LLC e1b49257-d226-457f-8f2d-9a757a65bbcb 2022-09-06 Warnings Exact identifier unii: WK2XYI10QM REFRESH OPTIVE Advanced CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, AND POLYSORBATE 80 Allergan, Inc. aaa943e4-7c38-4c5a-b7c0-5a656d8cafc0 2022-09-01 Warnings Exact identifier unii: PDC6A3C0OX unii: 6OZP39ZG8H unii: K679OBS311 Childrens Ibuprofen Oral Suspension IBUPROFEN Pharmaceutical Associates, Inc. 7a6832f2-2d80-483c-bde3-e6cacb7c318a 2022-08-31 Warnings Exact identifier rxcui: 197803 unii: WK2XYI10QM betr pain relief IBUPROFEN Live Betr LLC 1b709dce-5c71-45e6-b516-d510a0a8c25d 2022-08-24 Warnings Exact identifier unii: WK2XYI10QM Diphenhydramine HCl and Ibuprofen DIPHENHYDRAMINE HCL AND IBUPROFEN Aurohealth LLC 2c7c5349-06c9-401a-88e9-8f91ddb7f91a 2022-08-19 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen Oral IBUPROFEN ORAL Strategic Sourcing Services a3062142-db0e-4758-a762-2b2bb05670b1 2022-08-10 Warnings Exact identifier application number: ANDA210602 ndc (package): 70677-0150-2 ndc (package): 70677-0153-1 ndc (package): 70677-0152-1 ndc (package): 70677-0151-1 ndc (package): 70677-0150-1 ndc (product): 70677-0153 ndc (product): 70677-0152 ndc (product): 70677-0150 ndc (product): 70677-0151 ndc11 (package): 70677015201 rxcui: 197803 spl id: e5e79c54-bf94-3d7d-e053-2995a90a3812 spl set id: a3062142-db0e-4758-a762-2b2bb05670b1 unii: WK2XYI10QM Ibuprofen IBUPROFEN TABLET, FILM-COATED Lil' Drug Store Products, Inc. e5bf5e09-7d42-6314-e053-2a95a90a2325 2022-08-08 Warnings Exact identifier unii: WK2XYI10QM Glycerinum GLYCERINUM Hahnemann Laboratories, INC. e34f8796-85b5-2946-e053-2995a90a251e 2022-07-08 Exact identifier unii: PDC6A3C0OX Ibuprofen IBUPROFEN DOLGENCORP, INC. df321783-73cb-55bf-e053-2a95a90a4ce2 2022-07-07 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen IBUPROFEN Proficient Rx LP b7565aac-a928-4116-b9af-cf636da4537c 2022-07-01 Warnings Exact identifier rxcui: 197803 unii: WK2XYI10QM REFRESH TEARS CARBOXYMETHYLCELLULOSE SODIUM Allergan, Inc. 329d1fe0-4432-4565-b7b1-65666bd86526 2022-06-30 Warnings Exact identifier unii: K679OBS311 REFRESH Optive Mega-3 CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN AND POLYSORBATE 80 Allergan, Inc. c5f2b3f2-2071-45bd-a010-67f848bc0233 2022-06-30 Warnings Exact identifier unii: PDC6A3C0OX unii: 6OZP39ZG8H unii: K679OBS311 REFRESH PLUS CARBOXYMETHYLCELLULOSE SODIUM Allergan, Inc. 0f6a4b4b-cde6-4518-84b5-ce997f1154a7 2022-06-28 Warnings Exact identifier unii: K679OBS311 Sterile Water WATER Fresenius Kabi USA, LLC f42ac50f-0ec5-4713-a4c8-99d972d90bed 2022-06-22 Warnings, Adverse reactions Exact identifier unii: 059QF0KO0R Sterile Water WATER Fresenius Kabi USA, LLC e71c6c83-d518-496c-b2ab-efd5987e4783 2022-06-09 Warnings, Adverse reactions Exact identifier unii: 059QF0KO0R Ibuprofen and Diphenhydramine Citrate IBUPROFEN AND DIPHENHYDRAMINE CITRATE Aurohealth LLC 21c1f5c5-19fa-4a59-bad3-ea85fd37471b 2022-06-03 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen IBUPROFEN CARDINAL HEALTH dfbbde4f-633d-6d57-e053-2a95a90ad82f 2022-05-24 Warnings Exact identifier unii: WK2XYI10QM
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.