NDC 70518-1409 – Ibuprofen

Ibuprofen 800 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70518-1409

Product details

Brand name
Ibuprofen
Generic name
Ibuprofen
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091625
Marketed since
September 11, 2018
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibuprofen →

Package NDC codes (6)

Package NDCDescriptionSince
70518-1409-030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1409-0)Sep 11, 2018
70518-1409-121 TABLET, FILM COATED in 1 BLISTER PACK (70518-1409-1)Sep 14, 2018
70518-1409-290 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1409-2)Sep 17, 2018
70518-1409-430 TABLET, FILM COATED in 1 BLISTER PACK (70518-1409-4)Sep 24, 2018
70518-1409-510 TABLET, FILM COATED in 1 BLISTER PACK (70518-1409-5)Oct 8, 2018
70518-1409-920 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1409-9)May 20, 2021

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