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FDA NDC

ACAMPROSATE CALCIUM

This name is from the loaded FDA file.

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Source: FDA NDC Directory, live from openFDA. Publisher page

NDC
70069-860
Proprietary name
ACAMPROSATE CALCIUM
Nonproprietary name
ACAMPROSATE CALCIUM
Labeler
Somerset Therapeutics, LLC
Dosage form
TABLET, DELAYED RELEASE
Strength
333 mg/1

HCPCS J0132 Billable units per 11-digit NDC: 240.

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