MORPHINE SULFATE

NDC 67877-671 · Ascend Laboratories, LLC

Generic nameMORPHINE SULFATE

Dosage formTABLET

RouteORAL

Active ingredient(s)MORPHINE SULFATE

Strength30 mg/1

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

DEA scheduleCII

Marketing categoryANDA

Packages

67877-671-01 — 100 TABLET in 1 BOTTLE (67877-671-01)

FDA lists these products with the same active ingredient.

63629-2537 — MORPHINE SULFATE, 63629-2538 — MORPHINE SULFATE, 63629-4483 — Morphine Sulfate, 63629-4484 — Morphine Sulfate, 63629-8459 — MORPHINE SULFATE, 63629-8505 — Morphine Sulfate, 66794-160 — Morphine Sulfate, 66794-162 — Morphine Sulfate, 67296-2122 — Morphine Sulfate, 67877-670 — MORPHINE SULFATE, 68000-110 — Morphine Sulfate, 68000-111 — Morphine Sulfate, 68000-112 — Morphine Sulfate, 68000-113 — Morphine Sulfate, 68000-114 — Morphine Sulfate, 68084-157 — Morphine Sulfate, 68084-158 — Morphine Sulfate, 68094-001 — Morphine Sulfate, 68094-045 — Morphine Sulfate, 68094-056 — 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.