NDC 71335-1417 – Hydrocodone Bitartrate and Acetaminophen

Hydrocodone Bitartrate 5 mg/1; Acetaminophen 325 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC71335-1417

Product details

Brand name
Hydrocodone Bitartrate and Acetaminophen
Generic name
Hydrocodone Bitartrate and Acetaminophen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202991
Marketed since
April 12, 2016
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (10)

Package NDCDescriptionSince
71335-1417-010 TABLET in 1 BOTTLE (71335-1417-0)Jan 10, 2020
71335-1417-130 TABLET in 1 BOTTLE (71335-1417-1)Jan 14, 2020
71335-1417-2120 TABLET in 1 BOTTLE (71335-1417-2)Oct 2, 2020
71335-1417-320 TABLET in 1 BOTTLE (71335-1417-3)Dec 6, 2019
71335-1417-460 TABLET in 1 BOTTLE (71335-1417-4)Jan 21, 2020
71335-1417-590 TABLET in 1 BOTTLE (71335-1417-5)May 15, 2020
71335-1417-68 TABLET in 1 BOTTLE (71335-1417-6)Jul 9, 2024
71335-1417-740 TABLET in 1 BOTTLE (71335-1417-7)May 18, 2020
71335-1417-815 TABLET in 1 BOTTLE (71335-1417-8)Dec 9, 2019
71335-1417-984 TABLET in 1 BOTTLE (71335-1417-9)Jul 9, 2024

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