Skip to main content

acamprosate calcium

NDC 68382-569 · Zydus Pharmaceuticals (USA) Inc.

Generic nameacamprosate calcium
Dosage formTABLET, DELAYED RELEASE
RouteORAL
Active ingredient(s)ACAMPROSATE CALCIUM
Strength333 mg/1
Marketing categoryANDA

Packages

68382-569-01 — 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-01)

68382-569-05 — 500 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-05)

68382-569-06 — 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-06)

68382-569-10 — 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-10)

68382-569-16 — 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-16)

68382-569-28 — 180 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-28)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0378-6333 — acamprosate calcium enteric-coated, 0615-8560 — acamprosate calcium enteric-coated, 0904-7213 — Acamprosate Calcium, 60687-121 — Acamprosate Calcium, 68462-435 — Acamprosate Calcium, 69452-353 — Acamprosate Calcium, 70069-860 — ACAMPROSATE CALCIUM, 70518-4616 — acamprosate calcium, 70771-1057 — acamprosate calcium

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