NDC 71335-2818 – Acetaminophen and Codeine Phosphate

Acetaminophen 300 mg/1; Codeine Phosphate 60 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIII

Product NDC71335-2818

Product details

Brand name
Acetaminophen and Codeine Phosphate
Generic name
Acetaminophen and Codeine Phosphate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA089828
Marketed since
May 20, 2024
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Acetaminophen and Codeine Phosphate →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2818-0100 TABLET in 1 BOTTLE (71335-2818-0)Oct 22, 2025
71335-2818-130 TABLET in 1 BOTTLE (71335-2818-1)Oct 22, 2025
71335-2818-2120 TABLET in 1 BOTTLE (71335-2818-2)Oct 22, 2025
71335-2818-360 TABLET in 1 BOTTLE (71335-2818-3)Oct 22, 2025
71335-2818-490 TABLET in 1 BOTTLE (71335-2818-4)Oct 22, 2025
71335-2818-540 TABLET in 1 BOTTLE (71335-2818-5)Oct 22, 2025
71335-2818-620 TABLET in 1 BOTTLE (71335-2818-6)Oct 22, 2025
71335-2818-7112 TABLET in 1 BOTTLE (71335-2818-7)Oct 22, 2025
71335-2818-884 TABLET in 1 BOTTLE (71335-2818-8)Oct 22, 2025
71335-2818-915 TABLET in 1 BOTTLE (71335-2818-9)Oct 22, 2025

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