NDC 71335-1522 – Acetaminophen And Codeine Phosphate

Acetaminophen 300 mg/1; Codeine Phosphate 30 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIII

Product NDC71335-1522

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 · ANDA040419
Marketed since
May 31, 2001
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
71335-1522-040 TABLET in 1 BOTTLE (71335-1522-0)Aug 17, 2020
71335-1522-16 TABLET in 1 BOTTLE (71335-1522-1)Mar 13, 2020
71335-1522-220 TABLET in 1 BOTTLE (71335-1522-2)Mar 30, 2020
71335-1522-330 TABLET in 1 BOTTLE (71335-1522-3)Mar 5, 2020
71335-1522-484 TABLET in 1 BOTTLE (71335-1522-4)Apr 3, 2024
71335-1522-515 TABLET in 1 BOTTLE (71335-1522-5)Mar 6, 2020
71335-1522-6120 TABLET in 1 BOTTLE (71335-1522-6)Mar 3, 2020
71335-1522-7100 TABLET in 1 BOTTLE (71335-1522-7)Apr 3, 2024
71335-1522-860 TABLET in 1 BOTTLE (71335-1522-8)Feb 24, 2020
71335-1522-990 TABLET in 1 BOTTLE (71335-1522-9)Mar 6, 2020

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