Home NDC 67414-240-00 Motrin IB
Product NDC 67414-240
Requested package NDC 67414-240-00
11-digit product format 674140240
Labeler code 67414
Product ID 67414-240_ddd2849e-23ea-dd00-e053-2995a90a252f
Type HUMAN OTC DRUG
Nonproprietary name IBUPROFEN
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Jones Healthcare Group - Packaging Services, Inc
Application ANDA077349
Marketing category ANDA
Marketing start 2016-07-01
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 A077349-001 IBUPROFEN IBUPROFEN 200MG TABLET / ORAL RS 2005-06-21
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 A077349-001 IBUPROFEN 200MG TABLET / ORAL RS 2005-06-21 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 2 · 21 matching rows.
Additional Listing Data#
Finished product Yes
Brand name base Motrin IB
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 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 201126 Internal RxNorm lookup 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 67414-240-00 Motrin IB 2500 in 1 BOX TABLET, FILM COATED 2500 5 67414-240-00 Motrin IB 2 in 1 POUCH TABLET, FILM COATED 2 5 67414-240-09 Motrin IB 2 in 1 POUCH TABLET, FILM COATED 2 5 67414-240-09 Motrin IB 50 in 1 CARTON TABLET, FILM COATED 50 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67414-240 MOTRIN IB (IBUPROFEN) TABLET, FILM COATED [JONES HEALTHCARE GROUP - PACKAGING SERVICES, INC] 5 Current NDC, Legacy NDC, 4 package rows 20220430_6419cc78-27d4-7713-e053-2a91aa0a5a10.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 67414-240-00 67414024000 2500 POUCH in 1 BOX (67414-240-00) / 2 TABLET, FILM COATED in 1 POUCH 2500 pouch 2018-01-25 0000-00-00 No No Current