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Atorvastatin Calcium

NDC 59651-608 · Aurobindo Pharma Limited

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

59651-608-05 — 500 TABLET, FILM COATED in 1 BOTTLE (59651-608-05)

59651-608-30 — 30 TABLET, FILM COATED in 1 BOTTLE (59651-608-30)

59651-608-90 — 90 TABLET, FILM COATED in 1 BOTTLE (59651-608-90)

59651-608-99 — 1000 TABLET, FILM COATED in 1 BOTTLE (59651-608-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

58151-064 — amlodipine and atorvastatin, 58151-065 — amlodipine and atorvastatin, 58151-066 — amlodipine and atorvastatin, 58151-067 — amlodipine and atorvastatin, 58151-155 — atorvastatin calcium, 58151-156 — atorvastatin calcium, 58151-157 — atorvastatin calcium, 58151-158 — atorvastatin calcium, 59651-606 — Atorvastatin Calcium, 59651-607 — Atorvastatin Calcium, 59651-609 — Atorvastatin Calcium, 60505-3478 — Amlodipine and Atorvastatin, 60505-3479 — Amlodipine and Atorvastatin, 60505-3483 — Amlodipine and Atorvastatin, 60505-3484 — Amlodipine and Atorvastatin, 60505-3488 — Amlodipine and Atorvastatin, 60505-3489 — Amlodipine and Atorvastatin, 60505-3492 — Amlodipine and Atorvastatin, 60505-3493 — Amlodipine and Atorvastatin, 60760-666 — 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.