NDC 71335-2182 – Endocet

Oxycodone Hydrochloride 10 mg/1; Acetaminophen 325 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC71335-2182

Product details

Brand name
Endocet
Generic name
Oxycodone and Acetaminophen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040330
Marketed since
March 6, 2003
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Endocet →

Package NDC codes (9)

Package NDCDescriptionSince
71335-2182-130 TABLET in 1 BOTTLE (71335-2182-1)Oct 21, 2022
71335-2182-2120 TABLET in 1 BOTTLE (71335-2182-2)Oct 7, 2022
71335-2182-390 TABLET in 1 BOTTLE (71335-2182-3)Sep 7, 2022
71335-2182-428 TABLET in 1 BOTTLE (71335-2182-4)Aug 12, 2024
71335-2182-560 TABLET in 1 BOTTLE (71335-2182-5)Sep 28, 2022
71335-2182-620 TABLET in 1 BOTTLE (71335-2182-6)Aug 12, 2024
71335-2182-745 TABLET in 1 BOTTLE (71335-2182-7)Aug 12, 2024
71335-2182-875 TABLET in 1 BOTTLE (71335-2182-8)Aug 12, 2024
71335-2182-9100 TABLET in 1 BOTTLE (71335-2182-9)Aug 12, 2024

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