NDC 13107-004 – Hydrocodone Bitartrate and Ibuprofen

Hydrocodone Bitartrate 7.5 mg/1; Ibuprofen 200 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CII

Product NDC13107-004

Product details

Brand name
Hydrocodone Bitartrate and Ibuprofen
Generic name
Hydrocodone Bitartrate and Ibuprofen
Labeler
Aurolife Pharma, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204575
Marketed since
June 2, 2016
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug; Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Hydrocodone Bitartrate and Ibuprofen →

Package NDC codes (4)

Package NDCDescriptionSince
13107-004-01100 TABLET, FILM COATED in 1 BOTTLE (13107-004-01)Jun 2, 2016
13107-004-05500 TABLET, FILM COATED in 1 BOTTLE (13107-004-05)Jun 2, 2016
13107-004-1110 TABLET, FILM COATED in 1 BOTTLE (13107-004-11)Jun 2, 2016
13107-004-991000 TABLET, FILM COATED in 1 BOTTLE (13107-004-99)Jun 2, 2016

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