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ATORVASTATIN CALCIUM

NDC 71205-731 · Proficient Rx LP

Generic nameATORVASTATIN CALCIUM
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ATORVASTATIN CALCIUM TRIHYDRATE
Strength40 mg/1
Pharmacologic classHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Marketing categoryANDA

Packages

71205-731-30 — 30 TABLET, FILM COATED in 1 BOTTLE (71205-731-30)

71205-731-60 — 60 TABLET, FILM COATED in 1 BOTTLE (71205-731-60)

71205-731-90 — 90 TABLET, FILM COATED in 1 BOTTLE (71205-731-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70756-250 — Atorvastatin calcium, 70771-1875 — atorvastatin calcium, 70771-1876 — atorvastatin calcium, 70771-1877 — atorvastatin calcium, 70771-1878 — atorvastatin calcium, 71205-098 — Atorvastatin Calcium, 71205-246 — ATORVASTATIN CALCIUM, 71205-247 — ATORVASTATIN CALCIUM, 71205-264 — Atorvastatin Calcium, 71205-335 — Atorvastatin calcium, 71205-765 — Atorvastatin calcium, 71209-090 — Atorvastatin Calcium, 71209-091 — Atorvastatin Calcium, 71209-092 — Atorvastatin Calcium, 71209-093 — Atorvastatin Calcium, 71335-1010 — Atorvastatin Calcium, 71335-1011 — Atorvastatin Calcium, 71335-1126 — ATORVASTATIN CALCIUM, 71335-1336 — Atorvastatin calcium, 71335-1388 — ATORVASTATIN CALCIUM, +365 more

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