NDC 71335-2117 – Hydrocodone Bitartrate and Acetaminophen

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

Human Prescription Drug DEA schedule CII

Product NDC71335-2117

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
71335-2117-010 TABLET in 1 BOTTLE (71335-2117-0)Jun 20, 2022
71335-2117-130 TABLET in 1 BOTTLE (71335-2117-1)Jun 20, 2022
71335-2117-2120 TABLET in 1 BOTTLE (71335-2117-2)Jun 20, 2022
71335-2117-320 TABLET in 1 BOTTLE (71335-2117-3)Jun 20, 2022
71335-2117-460 TABLET in 1 BOTTLE (71335-2117-4)Jun 20, 2022
71335-2117-590 TABLET in 1 BOTTLE (71335-2117-5)Jun 20, 2022
71335-2117-650 TABLET in 1 BOTTLE (71335-2117-6)Jun 20, 2022
71335-2117-740 TABLET in 1 BOTTLE (71335-2117-7)Jun 20, 2022
71335-2117-815 TABLET in 1 BOTTLE (71335-2117-8)Jun 20, 2022
71335-2117-984 TABLET in 1 BOTTLE (71335-2117-9)Jun 20, 2022

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