acamprosate calcium

Generic: acamprosate calcium

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acamprosate calcium
Generic Name acamprosate calcium
Labeler american health packaging
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

acamprosate calcium 333 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-121
Product ID 60687-121_3d49a773-bfca-9870-e063-6294a90a2945
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202229
Listing Expiration 2026-12-31
Marketing Start 2015-10-27

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687121
Hyphenated Format 60687-121

Supplemental Identifiers

RxCUI
835726
UNII
59375N1D0U

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name acamprosate calcium (source: ndc)
Generic Name acamprosate calcium (source: ndc)
Application Number ANDA202229 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 333 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-121-25) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-121-95)
source: ndc

Packages (1)

Ingredients (1)

acamprosate calcium (333 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3d49a773-bfca-9870-e063-6294a90a2945", "openfda": {"unii": ["59375N1D0U"], "rxcui": ["835726"], "spl_set_id": ["94ef2a5c-cc2f-4e7f-b159-b2d38188d5b8"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-121-25)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-121-95)", "package_ndc": "60687-121-25", "marketing_start_date": "20151027"}], "brand_name": "Acamprosate Calcium", "product_id": "60687-121_3d49a773-bfca-9870-e063-6294a90a2945", "dosage_form": "TABLET, DELAYED RELEASE", "product_ndc": "60687-121", "generic_name": "Acamprosate Calcium", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acamprosate Calcium", "active_ingredients": [{"name": "ACAMPROSATE CALCIUM", "strength": "333 mg/1"}], "application_number": "ANDA202229", "marketing_category": "ANDA", "marketing_start_date": "20151027", "listing_expiration_date": "20261231"}