NDC 71335-3080 – Morphine sulfate

Morphine Sulfate 100 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC71335-3080

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, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
71335-3080-190 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3080-1)Feb 13, 2026
71335-3080-260 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3080-2)Feb 13, 2026
71335-3080-330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3080-3)Feb 13, 2026
71335-3080-4120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3080-4)Feb 13, 2026

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