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Atorvastatin Calcium

NDC 51655-747 · Northwind Health Company, LLC

Generic nameAtorvastatin Calcium
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ATORVASTATIN CALCIUM TRIHYDRATE
Strength80 mg/1
Pharmacologic classHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Marketing categoryANDA

Packages

51655-747-52 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-747-52)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50228-451 — ATORVASTATIN CALCIUM, 50228-452 — ATORVASTATIN CALCIUM, 50228-453 — ATORVASTATIN CALCIUM, 50228-454 — ATORVASTATIN CALCIUM, 51079-208 — atorvastatin calcium, 51079-209 — atorvastatin calcium, 51079-210 — atorvastatin calcium, 51079-211 — atorvastatin calcium, 51655-464 — Atorvastatin Calcium, 51655-465 — Atorvastatin Calcium, 51655-946 — ATORVASTATIN CALCIUM, 55111-121 — Atorvastatin Calcium, 55111-122 — Atorvastatin Calcium, 55111-123 — Atorvastatin Calcium, 55111-124 — Atorvastatin Calcium, 55154-0284 — atorvastatin calcium, 55154-4384 — atorvastatin calcium, 58151-062 — amlodipine and atorvastatin, 58151-063 — amlodipine and atorvastatin, 58151-064 — amlodipine and atorvastatin, +365 more

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