Home NDC 70436-182 Ibuprofen
Product NDC 70436-182
11-digit product format 704360182
Labeler code 70436
Product ID 70436-182_ee2fa6b8-1588-13e1-e053-2995a90a6aa0
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Ibuprofen
Dosage form TABLET
Route ORAL
Labeler Slate Run Pharmaceuticals, LLC
Application ANDA215318
Marketing category ANDA
Marketing start 2022-07-25
Marketing end 0000-00-00
Substance IBUPROFEN
Active strength 800 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 2023-12-31
Current FDA listing Historical FDA.report record 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 · 27 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 A215318-001 IBUPROFEN IBUPROFEN 400MG TABLET / ORAL AB 2022-03-30 A215318-002 IBUPROFEN IBUPROFEN 600MG TABLET / ORAL AB 2022-03-30 A215318-003 IBUPROFEN IBUPROFEN 800MG TABLET / ORAL AB 2022-03-30
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 3 · 96 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 A215318-001 IBUPROFEN 400MG TABLET / ORAL AB 2022-03-30 84e616aacf4f…2026-09-14 22:38:34 2026-08 A215318-002 IBUPROFEN 600MG TABLET / ORAL AB 2022-03-30 84e616aacf4f…2026-09-14 22:38:34 2026-08 A215318-003 IBUPROFEN 800MG TABLET / ORAL AB 2022-03-30 84e616aacf4f…2026-08-18 06:07:40 2026-07 A215318-001 IBUPROFEN 400MG TABLET / ORAL AB 2022-03-30 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A215318-002 IBUPROFEN 600MG TABLET / ORAL AB 2022-03-30 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A215318-003 IBUPROFEN 800MG TABLET / ORAL AB 2022-03-30 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A215318-001 IBUPROFEN 400MG TABLET / ORAL AB 2022-03-30 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A215318-002 IBUPROFEN 600MG TABLET / ORAL AB 2022-03-30 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A215318-003 IBUPROFEN 800MG TABLET / ORAL AB 2022-03-30 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A215318-001 IBUPROFEN 400MG TABLET / ORAL AB 2022-03-30 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A215318-002 IBUPROFEN 600MG TABLET / ORAL AB 2022-03-30 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A215318-003 IBUPROFEN 800MG TABLET / ORAL AB 2022-03-30 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A215318-001 IBUPROFEN 400MG TABLET / ORAL AB 2022-03-30 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A215318-002 IBUPROFEN 600MG TABLET / ORAL AB 2022-03-30 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A215318-003 IBUPROFEN 800MG TABLET / ORAL AB 2022-03-30 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A215318-001 IBUPROFEN 400MG TABLET / ORAL AB 2022-03-30 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A215318-002 IBUPROFEN 600MG TABLET / ORAL AB 2022-03-30 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A215318-003 IBUPROFEN 800MG TABLET / ORAL AB 2022-03-30 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A215318-001 IBUPROFEN 400MG TABLET / ORAL AB 2022-03-30 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A215318-002 IBUPROFEN 600MG TABLET / ORAL AB 2022-03-30 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A215318-003 IBUPROFEN 800MG TABLET / ORAL AB 2022-03-30 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A215318-001 IBUPROFEN 400MG TABLET / ORAL AB 2022-03-30 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A215318-002 IBUPROFEN 600MG TABLET / ORAL AB 2022-03-30 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A215318-003 IBUPROFEN 800MG TABLET / ORAL AB 2022-03-30 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A215318-001 IBUPROFEN 400MG TABLET / ORAL AB 2022-03-30 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A215318-002 IBUPROFEN 600MG TABLET / ORAL AB 2022-03-30 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A215318-003 IBUPROFEN 800MG TABLET / ORAL AB 2022-03-30 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A215318-001 IBUPROFEN 400MG TABLET / ORAL AB 2022-03-30 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A215318-002 IBUPROFEN 600MG TABLET / ORAL AB 2022-03-30 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A215318-003 IBUPROFEN 800MG TABLET / ORAL AB 2022-03-30 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A215318-001 IBUPROFEN 400MG TABLET / ORAL AB 2022-03-30 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A215318-002 IBUPROFEN 600MG TABLET / ORAL AB 2022-03-30 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A215318-003 IBUPROFEN 800MG TABLET / ORAL AB 2022-03-30 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 A215318-001 IBUPROFEN 400MG TABLET / ORAL AB 2022-03-30 d06236e962d9…2024-10-29 15:01 UTC 2024-10 A215318-002 IBUPROFEN 600MG TABLET / ORAL AB 2022-03-30 d06236e962d9…2024-10-29 15:01 UTC 2024-10 A215318-003 IBUPROFEN 800MG TABLET / ORAL AB 2022-03-30 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A215318-001 IBUPROFEN 400MG TABLET / ORAL AB 2022-03-30 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A215318-002 IBUPROFEN 600MG TABLET / ORAL AB 2022-03-30 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A215318-003 IBUPROFEN 800MG TABLET / ORAL AB 2022-03-30 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A215318-001 IBUPROFEN 400MG TABLET / ORAL AB 2022-03-30 301d65b070ca…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 3 · 96 observed states.
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 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Ibuprofen IBUPROFEN Westminster Pharmaceuticals, LLC 6f7e255f-48c9-4366-8725-7f8cbe1bb75a 2026-03-20 Boxed warning, Warnings, Adverse reactions Exact identifier application applno (ANDA): 215318 application number: ANDA215318
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70436-182-01 70436018201 100 TABLET in 1 BOTTLE (70436-182-01) 100 tablet 2022-07-25 0000-00-00 No No Current 70436-182-02 70436018202 500 TABLET in 1 BOTTLE (70436-182-02) 500 tablet 2022-07-25 0000-00-00 No No Current