NDC 71335-2115 – Hydrocodone Bitartrate and Acetaminophen

Hydrocodone Bitartrate 7.5 mg/1; Acetaminophen 325 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC71335-2115

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 · ANDA211487
Marketed since
November 8, 2018
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
71335-2115-08 TABLET in 1 BOTTLE (71335-2115-0)Jun 20, 2022
71335-2115-1120 TABLET in 1 BOTTLE (71335-2115-1)Jun 20, 2022
71335-2115-215 TABLET in 1 BOTTLE (71335-2115-2)Jun 20, 2022
71335-2115-320 TABLET in 1 BOTTLE (71335-2115-3)Jun 20, 2022
71335-2115-428 TABLET in 1 BOTTLE (71335-2115-4)Jun 20, 2022
71335-2115-530 TABLET in 1 BOTTLE (71335-2115-5)Jun 20, 2022
71335-2115-640 TABLET in 1 BOTTLE (71335-2115-6)Jun 20, 2022
71335-2115-756 TABLET in 1 BOTTLE (71335-2115-7)Jun 20, 2022
71335-2115-860 TABLET in 1 BOTTLE (71335-2115-8)Jun 20, 2022
71335-2115-990 TABLET in 1 BOTTLE (71335-2115-9)Jun 20, 2022

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