Skip to main content

PRAVASTATIN SODIUM

NDC 16729-010 · Accord Healthcare Inc.

Generic namePRAVASTATIN SODIUM
Dosage formTABLET
RouteORAL
Active ingredient(s)PRAVASTATIN SODIUM
Strength40 mg/1
Pharmacologic classHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Marketing categoryANDA

Packages

16729-010-15 — 90 TABLET in 1 BOTTLE (16729-010-15)

16729-010-16 — 500 TABLET in 1 BOTTLE (16729-010-16)

16729-010-17 — 1000 TABLET in 1 BOTTLE (16729-010-17)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0615-8621 — PRAVASTATIN SODIUM, 0904-5891 — PRAVASTATIN SODIUM, 0904-5892 — PRAVASTATIN SODIUM, 0904-5893 — PRAVASTATIN SODIUM, 16714-558 — Pravastatin Sodium, 16714-559 — Pravastatin Sodium, 16714-560 — Pravastatin Sodium, 16714-570 — Pravastatin Sodium, 16729-008 — PRAVASTATIN SODIUM, 16729-009 — PRAVASTATIN SODIUM, 16729-011 — PRAVASTATIN SODIUM, 35356-919 — pravastatin sodium, 43063-807 — PRAVASTATIN SODIUM, 43063-808 — PRAVASTATIN SODIUM, 48433-148 — Pravastatin sodium, 48433-149 — Pravastatin sodium, 50090-0973 — Pravastatin Sodium, 50090-0975 — Pravastatin Sodium, 50090-1533 — Pravastatin Sodium, 50090-1594 — Pravastatin Sodium, +170 more

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