NDC 71335-0336 – Acetaminophen and Codeine Phosphate

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

Human Prescription Drug DEA schedule CIII

Product NDC71335-0336

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 · ANDA202800
Marketed since
April 15, 2013
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
71335-0336-0100 TABLET in 1 BOTTLE (71335-0336-0)Aug 9, 2024
71335-0336-130 TABLET in 1 BOTTLE (71335-0336-1)May 9, 2018
71335-0336-2120 TABLET in 1 BOTTLE (71335-0336-2)Aug 9, 2024
71335-0336-360 TABLET in 1 BOTTLE (71335-0336-3)Feb 12, 2018
71335-0336-490 TABLET in 1 BOTTLE (71335-0336-4)Aug 9, 2024
71335-0336-540 TABLET in 1 BOTTLE (71335-0336-5)Aug 9, 2024
71335-0336-620 TABLET in 1 BOTTLE (71335-0336-6)Mar 29, 2018
71335-0336-7112 TABLET in 1 BOTTLE (71335-0336-7)Aug 9, 2024
71335-0336-884 TABLET in 1 BOTTLE (71335-0336-8)Aug 9, 2024
71335-0336-915 TABLET in 1 BOTTLE (71335-0336-9)Aug 9, 2024

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