NDC 71335-0736 – Morphine sulfate

Morphine Sulfate 15 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC71335-0736

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
71335-0736-026 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-0)Apr 3, 2024
71335-0736-130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-1)Mar 16, 2018
71335-0736-260 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-2)Mar 28, 2018
71335-0736-390 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-3)Apr 13, 2018
71335-0736-4120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-4)Apr 3, 2024
71335-0736-540 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-5)Apr 3, 2024
71335-0736-614 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-6)Apr 3, 2024
71335-0736-715 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-7)Apr 3, 2024
71335-0736-820 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-8)Apr 3, 2024
71335-0736-984 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0736-9)Apr 3, 2024

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