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Quetiapine

NDC 67877-249 · Ascend Laboratories, LLC

Generic nameQuetiapine
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)QUETIAPINE FUMARATE
Strength50 mg/1
Pharmacologic classAtypical Antipsychotic [EPC]
Marketing categoryANDA

Packages

67877-249-01 — 100 TABLET, FILM COATED in 1 BOTTLE (67877-249-01)

67877-249-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (67877-249-10)

67877-249-33 — 1 BLISTER PACK in 1 CARTON (67877-249-33) / 10 TABLET, FILM COATED in 1 BLISTER PACK

67877-249-38 — 10 BLISTER PACK in 1 CARTON (67877-249-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67046-1116 — quetiapine, 67046-1440 — Quetiapine fumarate, 67046-1588 — Quetiapine Fumarate, 67046-1623 — Quetiapine, 67046-1649 — Quetiapine Fumarate, 67877-242 — Quetiapine, 67877-245 — Quetiapine, 67877-246 — Quetiapine, 67877-247 — Quetiapine, 67877-248 — Quetiapine, 67877-250 — Quetiapine, 68001-180 — quetiapine, 68001-181 — quetiapine, 68001-182 — quetiapine, 68001-183 — quetiapine, 68001-184 — quetiapine, 68001-185 — quetiapine, 68001-598 — Quetiapine, 68001-599 — Quetiapine, 68001-600 — Quetiapine, +323 more

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