NDC 63187-614 – Ibu

Ibuprofen 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63187-614

Product details

Brand name
Ibu
Generic name
Ibuprofen
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075682
Marketed since
November 20, 2008
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Ibu →

Package NDC codes (10)

Package NDCDescriptionSince
63187-614-1515 TABLET in 1 BOTTLE (63187-614-15)Jan 1, 2016
63187-614-2020 TABLET in 1 BOTTLE (63187-614-20)Mar 1, 2017
63187-614-2121 TABLET in 1 BOTTLE (63187-614-21)Dec 11, 2025
63187-614-2828 TABLET in 1 BOTTLE (63187-614-28)Oct 1, 2019
63187-614-3030 TABLET in 1 BOTTLE (63187-614-30)Jan 1, 2016
63187-614-4040 TABLET in 1 BOTTLE (63187-614-40)Jun 1, 2017
63187-614-4242 TABLET in 1 BOTTLE (63187-614-42)Feb 21, 2020
63187-614-4545 TABLET in 1 BOTTLE (63187-614-45)Jan 1, 2016
63187-614-6060 TABLET in 1 BOTTLE (63187-614-60)Jan 1, 2016
63187-614-9090 TABLET in 1 BOTTLE (63187-614-90)Jan 1, 2016

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