Morphine sulfate

NDC 63304-451 · Sun Pharmaceutical Industries, Inc.

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

63304-451-01 — 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-451-01)

63304-451-03 — 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-451-03)

63304-451-05 — 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-451-05)

FDA lists these products with the same active ingredient.

43386-540 — Morphine Sulfate, 43386-541 — Morphine Sulfate, 43386-542 — Morphine Sulfate, 43386-543 — Morphine Sulfate, 43386-544 — Morphine Sulfate, 60687-617 — Morphine Sulfate, 60687-760 — Morphine Sulfate, 60687-927 — MORPHINE SULFATE, 60760-893 — MORPHINE SULFATE, 63304-450 — morphine sulfate, 63304-452 — morphine sulfate, 63304-453 — morphine sulfate, 63304-758 — morphine sulfate, 63323-451 — Morphine Sulfate, 63323-452 — Morphine Sulfate, 63323-454 — Morphine Sulfate, 63323-455 — Morphine Sulfate, 63323-458 — Morphine Sulfate, 63629-1087 — morphine sulfate, 63629-1088 — 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.