Morphine sulfate

NDC 71335-3080 · Bryant Ranch Prepack

Generic namemorphine sulfate

Dosage formTABLET, FILM COATED, EXTENDED RELEASE

RouteORAL

Active ingredient(s)MORPHINE SULFATE

Strength100 mg/1

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

DEA scheduleCII

Marketing categoryANDA

Packages

71335-3080-1 — 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3080-1)

71335-3080-2 — 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3080-2)

71335-3080-3 — 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3080-3)

71335-3080-4 — 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3080-4)

FDA lists these products with the same active ingredient.

68094-001 — Morphine Sulfate, 68094-045 — Morphine Sulfate, 68094-056 — Morphine Sulfate, 68094-156 — Morphine Sulfate, 68094-256 — Morphine Sulfate, 68094-356 — Morphine Sulfate, 68094-556 — Morphine Sulfate, 71335-0676 — morphine sulfate, 71335-0707 — morphine sulfate, 71335-0736 — morphine sulfate, 71335-9662 — MORPHINE SULFATE, 72162-1282 — Morphine Sulfate, 72162-1352 — Morphine Sulfate, 72162-1789 — morphine sulfate, 72162-1790 — morphine sulfate, 72162-1791 — morphine sulfate, 72162-1792 — morphine sulfate, 72162-1793 — morphine sulfate, 72572-440 — Morphine Sulfate, 75826-129 — Morphine Sulfate, +129 more

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