NDC 71335-1818 – Acetaminophen And Codeine Phosphate

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

Human Prescription Drug DEA schedule CIII

Product NDC71335-1818

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 · ANDA211610
Marketed since
August 2, 2019
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (10)

Package NDCDescriptionSince
71335-1818-040 TABLET in 1 BOTTLE (71335-1818-0)Oct 7, 2024
71335-1818-16 TABLET in 1 BOTTLE (71335-1818-1)Oct 7, 2024
71335-1818-220 TABLET in 1 BOTTLE (71335-1818-2)Apr 20, 2021
71335-1818-330 TABLET in 1 BOTTLE (71335-1818-3)Apr 21, 2021
71335-1818-484 TABLET in 1 BOTTLE (71335-1818-4)Oct 7, 2024
71335-1818-515 TABLET in 1 BOTTLE (71335-1818-5)May 4, 2021
71335-1818-6120 TABLET in 1 BOTTLE (71335-1818-6)Oct 7, 2024
71335-1818-7100 TABLET in 1 BOTTLE (71335-1818-7)Mar 25, 2021
71335-1818-860 TABLET in 1 BOTTLE (71335-1818-8)Apr 28, 2021
71335-1818-990 TABLET in 1 BOTTLE (71335-1818-9)Apr 29, 2021

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