Morphine sulfate

NDC 72162-1790 · Bryant Ranch Prepack

Generic namemorphine sulfate

Dosage formTABLET, FILM COATED, EXTENDED RELEASE

RouteORAL

Active ingredient(s)MORPHINE SULFATE

Strength30 mg/1

Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]

DEA scheduleCII

Marketing categoryANDA

Packages

72162-1790-1 — 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1790-1)

72162-1790-3 — 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1790-3)

72162-1790-6 — 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1790-6)

72162-1790-9 — 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1790-9)

FDA lists these products with the same active ingredient.

68094-356 — Morphine Sulfate, 68094-556 — Morphine Sulfate, 71335-0676 — morphine sulfate, 71335-0707 — morphine sulfate, 71335-0736 — morphine sulfate, 71335-3080 — morphine sulfate, 71335-9662 — MORPHINE SULFATE, 72162-1282 — Morphine Sulfate, 72162-1352 — Morphine Sulfate, 72162-1789 — morphine sulfate, 72162-1791 — morphine sulfate, 72162-1792 — morphine sulfate, 72162-1793 — morphine sulfate, 72572-440 — Morphine Sulfate, 75826-129 — Morphine Sulfate, 75826-130 — Morphine Sulfate, 75826-131 — Morphine Sulfate, 76045-004 — Morphine Sulfate, 76045-005 — Morphine Sulfate, 76045-006 — Morphine Sulfate, +129 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.