Home NDC 11673-991 IBUPROFEN
Product NDC 11673-991
11-digit product format 116730991
Labeler code 11673
Product ID 11673-991_0e071c42-0f7e-586e-e063-6394a90a9533
Type HUMAN OTC DRUG
Nonproprietary name IBUPROFEN
Dosage form TABLET, COATED
Route ORAL
Labeler TARGET CORPORATION
Application ANDA091239
Marketing category ANDA
Marketing start 2020-02-04
Substance IBUPROFEN
Active strength 200 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 2026-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 1 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A091239-001 IBUPROFEN IBUPROFEN 200MG TABLET / ORAL 2011-02-01
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.
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 2026-08-01 22:54:32 2026-06 A091239-001 IBUPROFEN 200MG TABLET / ORAL 2011-02-01 a50c72e98297…
openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 1 · 16 matching rows.
Additional Listing Data#
Finished product Yes
Brand name base IBUPROFEN
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength IBUPROFEN 200 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 310965 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 11673-991-01 IBUPROFEN 100 in 1 BOTTLE TABLET, COATED 100 8 11673-991-05 IBUPROFEN 50 in 1 BOTTLE TABLET, COATED 50 8 11673-991-20 IBUPROFEN 200 in 1 BOTTLE TABLET, COATED 200 8 11673-991-50 IBUPROFEN 500 in 1 BOTTLE TABLET, COATED 500 8 11673-991-88 IBUPROFEN 1000 in 1 BOTTLE TABLET, COATED 1000 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11673-991 IBUPROFEN TABLET, COATED [TARGET CORPORATION] 8 Current NDC, Legacy NDC, 5 package rows 20240104_8e86ae68-7687-79d6-e053-2995a90ac274.zip
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 11673-991-01 11673099101 100 TABLET, COATED in 1 BOTTLE (11673-991-01) 2020-02-04 0000-00-00 No No Current 11673-991-05 11673099105 50 TABLET, COATED in 1 BOTTLE (11673-991-05) 2020-02-04 0000-00-00 No No Current 11673-991-20 11673099120 200 TABLET, COATED in 1 BOTTLE (11673-991-20) 2020-02-04 0000-00-00 No No Current 11673-991-50 11673099150 500 TABLET, COATED in 1 BOTTLE (11673-991-50) 2020-02-04 0000-00-00 No No Current 11673-991-88 11673099188 1000 TABLET, COATED in 1 BOTTLE (11673-991-88) 2020-02-04 0000-00-00 No No Current