Home NDC 69842-709 ibuprofen
Product NDC 69842-709
11-digit product format 698420709
Labeler code 69842
Product ID 69842-709_19adf0e9-5e97-4cc7-b637-e7e46d26d526
Type HUMAN OTC DRUG
Nonproprietary name Ibuprofen
Dosage form TABLET, FILM COATED
Route ORAL
Labeler CVS Pharmacy
Application ANDA206581
Marketing category ANDA
Marketing start 2018-02-02
Marketing end 0000-00-00
Substance IBUPROFEN SODIUM
Active strength 256 mg/1
NDC exclude flag No
Listing certified through 2020-12-31
Current FDA listing Historical FDA.report record 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 A206581-001 IBUPROFEN SODIUM IBUPROFEN SODIUM EQ 200MG BASE TABLET / ORAL 2015-08-03
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 A206581-001 IBUPROFEN SODIUM EQ 200MG BASE TABLET / ORAL 2015-08-03 a50c72e98297…