NDC 76420-821 – Acetaminophen And Codeine Phosphate

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

Human Prescription Drug DEA schedule CIII

Product NDC76420-821

Product details

Brand name
Acetaminophen And Codeine Phosphate
Generic name
acetaminophen and codeine phosphate
Labeler
Asclemed USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211610
Marketed since
August 2, 2019
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 (13)

Package NDCDescriptionSince
76420-821-00100 TABLET in 1 BOTTLE (76420-821-00)Jul 1, 2024
76420-821-011 TABLET in 1 BOTTLE (76420-821-01)Jul 1, 2024
76420-821-033 TABLET in 1 BOTTLE (76420-821-03)Jul 1, 2024
76420-821-055 TABLET in 1 BOTTLE (76420-821-05)Jul 1, 2024
76420-821-1010 TABLET in 1 BOTTLE (76420-821-10)Jul 1, 2024
76420-821-1212 TABLET in 1 BOTTLE (76420-821-12)Jul 1, 2024
76420-821-1515 TABLET in 1 BOTTLE (76420-821-15)Jul 1, 2024
76420-821-2020 TABLET in 1 BOTTLE (76420-821-20)Jul 1, 2024
76420-821-2424 TABLET in 1 BOTTLE (76420-821-24)Aug 17, 2025
76420-821-3030 TABLET in 1 BOTTLE (76420-821-30)Jul 1, 2024
76420-821-50500 TABLET in 1 BOTTLE (76420-821-50)Jul 1, 2024
76420-821-6060 TABLET in 1 BOTTLE (76420-821-60)Jul 1, 2024
76420-821-9090 TABLET in 1 BOTTLE (76420-821-90)Jul 1, 2024

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