NDC 71335-0676 – Morphine sulfate

Morphine Sulfate 30 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC71335-0676

Product details

Brand name
Morphine sulfate
Generic name
Morphine sulfate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078761
Marketed since
May 11, 2012
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Morphine Sulfate →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0676-040 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0676-0)Apr 3, 2024
71335-0676-130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0676-1)Feb 26, 2018
71335-0676-260 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0676-2)Feb 20, 2018
71335-0676-390 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0676-3)Mar 9, 2018
71335-0676-4120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0676-4)Apr 3, 2024
71335-0676-5100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0676-5)Apr 3, 2024
71335-0676-65 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0676-6)Apr 3, 2024
71335-0676-715 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0676-7)Apr 3, 2024
71335-0676-820 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0676-8)Apr 3, 2024
71335-0676-926 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0676-9)Apr 3, 2024

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