Home NDC 70518-0761 Ibuprofen
Product NDC 70518-0761
11-digit product format 705180761
Labeler code 70518
Product ID 70518-0761_557ab103-963d-f7b5-e063-6394a90aac5b
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Ibuprofen
Dosage form TABLET, FILM COATED
Route ORAL
Labeler REMEDYREPACK INC.
Application ANDA091625
Marketing category ANDA
Marketing start 2017-10-06
Substance IBUPROFEN
Active strength 600 mg/1
Pharmacologic classes Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes
Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 23 matching rows.
View current auxiliary records. · View the auxiliary file history.
Source provenance: Browse the complete Orange Book source catalog · source snapshot 43 .
Orange Book products# Current product rows page 1 of 1 · 3 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A091625-001 IBUPROFEN IBUPROFEN 400MG TABLET / ORAL AB 2015-09-15 A091625-002 IBUPROFEN IBUPROFEN 600MG TABLET / ORAL AB 2015-09-15 A091625-003 IBUPROFEN IBUPROFEN 800MG TABLET / ORAL AB 2015-09-15
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 3 matching rows.
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Product history page 1 of 4 · 129 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-09-14 22:38:34 2026-08 A091625-001 IBUPROFEN 400MG TABLET / ORAL AB 2015-09-15 84e616aacf4f…2026-09-14 22:38:34 2026-08 A091625-002 IBUPROFEN 600MG TABLET / ORAL AB 2015-09-15 84e616aacf4f…2026-09-14 22:38:34 2026-08 A091625-003 IBUPROFEN 800MG TABLET / ORAL AB 2015-09-15 84e616aacf4f…2026-08-18 06:07:40 2026-07 A091625-001 IBUPROFEN 400MG TABLET / ORAL AB 2015-09-15 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A091625-002 IBUPROFEN 600MG TABLET / ORAL AB 2015-09-15 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A091625-003 IBUPROFEN 800MG TABLET / ORAL AB 2015-09-15 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A091625-001 IBUPROFEN 400MG TABLET / ORAL AB 2015-09-15 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A091625-002 IBUPROFEN 600MG TABLET / ORAL AB 2015-09-15 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A091625-003 IBUPROFEN 800MG TABLET / ORAL AB 2015-09-15 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A091625-001 IBUPROFEN 400MG TABLET / ORAL AB 2015-09-15 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A091625-002 IBUPROFEN 600MG TABLET / ORAL AB 2015-09-15 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A091625-003 IBUPROFEN 800MG TABLET / ORAL AB 2015-09-15 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A091625-001 IBUPROFEN 400MG TABLET / ORAL AB 2015-09-15 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A091625-002 IBUPROFEN 600MG TABLET / ORAL AB 2015-09-15 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A091625-003 IBUPROFEN 800MG TABLET / ORAL AB 2015-09-15 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A091625-001 IBUPROFEN 400MG TABLET / ORAL AB 2015-09-15 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A091625-002 IBUPROFEN 600MG TABLET / ORAL AB 2015-09-15 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A091625-003 IBUPROFEN 800MG TABLET / ORAL AB 2015-09-15 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A091625-001 IBUPROFEN 400MG TABLET / ORAL AB 2015-09-15 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A091625-002 IBUPROFEN 600MG TABLET / ORAL AB 2015-09-15 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A091625-003 IBUPROFEN 800MG TABLET / ORAL AB 2015-09-15 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A091625-001 IBUPROFEN 400MG TABLET / ORAL AB 2015-09-15 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A091625-002 IBUPROFEN 600MG TABLET / ORAL AB 2015-09-15 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A091625-003 IBUPROFEN 800MG TABLET / ORAL AB 2015-09-15 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A091625-001 IBUPROFEN 400MG TABLET / ORAL AB 2015-09-15 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A091625-002 IBUPROFEN 600MG TABLET / ORAL AB 2015-09-15 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A091625-003 IBUPROFEN 800MG TABLET / ORAL AB 2015-09-15 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A091625-001 IBUPROFEN 400MG TABLET / ORAL AB 2015-09-15 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A091625-002 IBUPROFEN 600MG TABLET / ORAL AB 2015-09-15 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A091625-003 IBUPROFEN 800MG TABLET / ORAL AB 2015-09-15 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A091625-001 IBUPROFEN 400MG TABLET / ORAL AB 2015-09-15 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A091625-002 IBUPROFEN 600MG TABLET / ORAL AB 2015-09-15 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A091625-003 IBUPROFEN 800MG TABLET / ORAL AB 2015-09-15 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 A091625-001 IBUPROFEN 400MG TABLET / ORAL AB 2015-09-15 d06236e962d9…2024-10-29 15:01 UTC 2024-10 A091625-002 IBUPROFEN 600MG TABLET / ORAL AB 2015-09-15 d06236e962d9…2024-10-29 15:01 UTC 2024-10 A091625-003 IBUPROFEN 800MG TABLET / ORAL AB 2015-09-15 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A091625-001 IBUPROFEN 400MG TABLET / ORAL AB 2015-09-15 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A091625-002 IBUPROFEN 600MG TABLET / ORAL AB 2015-09-15 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A091625-003 IBUPROFEN 800MG TABLET / ORAL AB 2015-09-15 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A091625-001 IBUPROFEN 400MG TABLET / ORAL AB 2015-09-15 301d65b070ca…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 4 · 129 observed states.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Ibuprofen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength IBUPROFEN 600 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination WK2XYI10QM Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 197806 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70518-0761-0 Ibuprofen 20 in 1 BLISTER PACK TABLET, FILM COATED 20 23 70518-0761-1 Ibuprofen 30 in 1 BLISTER PACK TABLET, FILM COATED 30 23 70518-0761-2 Ibuprofen 28 in 1 BLISTER PACK TABLET, FILM COATED 28 23 70518-0761-3 Ibuprofen 21 in 1 BLISTER PACK TABLET, FILM COATED 21 23 70518-0761-4 Ibuprofen 15 in 1 BLISTER PACK TABLET, FILM COATED 15 23 70518-0761-5 Ibuprofen 10 in 1 BLISTER PACK TABLET, FILM COATED 10 23 70518-0761-6 Ibuprofen 90 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 90 23 70518-0761-7 Ibuprofen 60 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 60 23
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70518-0761 IBUPROFEN TABLET, FILM COATED [REMEDYREPACK INC.] 18 Current NDC, Legacy NDC, 8 package rows 20250429_1e6f3ce7-e8a3-40e8-8437-523ef5277b2e.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 3 of 3 · 41 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Ibuprofen IBUPROFEN Aphena Pharma Solutions - Tennessee, LLC 4a86a190-da5d-4b7a-a05f-e3e7ccbfa603 2019-01-19 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 091625 application number: ANDA091625
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 70518-0761-0 70518076100 20 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-0) 2017-10-06 0000-00-00 No No Current 70518-0761-1 70518076101 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-1) 2017-10-06 0000-00-00 No No Current 70518-0761-2 70518076102 28 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-2) 2018-07-26 0000-00-00 No No Current 70518-0761-3 70518076103 21 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-3) 2018-07-27 0000-00-00 No No Current 70518-0761-4 70518076104 15 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-4) 2018-07-30 0000-00-00 No No Current 70518-0761-5 70518076105 10 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-5) 2018-09-17 0000-00-00 No No Current 70518-0761-6 70518076106 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0761-6) 2019-07-09 0000-00-00 No No Current 70518-0761-7 70518076107 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0761-7) 2019-10-16 0000-00-00 No No Current