NDC 72162-1789 – Morphine sulfate

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

Human Prescription Drug DEA schedule CII

Product NDC72162-1789

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 (4)

Package NDCDescriptionSince
72162-1789-1100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1789-1)May 11, 2012
72162-1789-330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1789-3)May 11, 2012
72162-1789-660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1789-6)May 11, 2012
72162-1789-990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1789-9)May 11, 2012

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