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Pirfenidone

NDC 70954-869 · ANI Pharmaceuticals, Inc.

Generic namePirfenidone
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)PIRFENIDONE
Strength267 mg/1
Pharmacologic classPyridone [EPC], Pyridones [CS]
Marketing categoryANDA

Packages

70954-869-10 — 3 BOTTLE in 1 CARTON (70954-869-10) / 90 TABLET, FILM COATED in 1 BOTTLE

70954-869-30 — 270 TABLET, FILM COATED in 1 BOTTLE (70954-869-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60505-4681 — Pirfenidone, 60505-4682 — Pirfenidone, 62332-479 — Pirfenidone, 62332-480 — Pirfenidone, 69097-940 — PIRFENIDONE, 69097-987 — Pirfenidone, 69097-988 — Pirfenidone, 69238-1640 — Pirfenidone, 69238-1641 — Pirfenidone, 69238-1642 — Pirfenidone, 70954-870 — Pirfenidone, 71335-2944 — Pirfenidone, 71335-2984 — Pirfenidone, 72162-2465 — Pirfenidone, 72162-2466 — Pirfenidone, 72205-181 — PIRFENIDONE, 72205-182 — PIRFENIDONE, 72603-258 — PIRFENIDONE, 72603-259 — PIRFENIDONE, 76282-715 — PIRFENIDONE, +40 more

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