acamprosate calcium
Generic: acamprosate calcium
Labeler: zydus pharmaceuticals (usa) inc.Drug Facts
Product Profile
Brand Name
acamprosate calcium
Generic Name
acamprosate calcium
Labeler
zydus pharmaceuticals (usa) inc.
Dosage Form
TABLET, DELAYED RELEASE
Routes
Active Ingredients
acamprosate calcium 333 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68382-569
Product ID
68382-569_2e5f04a0-3e2d-494f-837b-18570b6a8546
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205995
Listing Expiration
2026-12-31
Marketing Start
2017-06-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68382569
Hyphenated Format
68382-569
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA205995 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 333 mg/1
Packaging
- 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-01)
- 500 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-05)
- 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-06)
- 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-10)
- 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-16)
- 180 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-28)
Packages (6)
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)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2e5f04a0-3e2d-494f-837b-18570b6a8546", "openfda": {"unii": ["59375N1D0U"], "rxcui": ["835726"], "spl_set_id": ["9803db35-2600-4f42-80c1-43216fd1ba3d"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-01)", "package_ndc": "68382-569-01", "marketing_start_date": "20170601"}, {"sample": false, "description": "500 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-05)", "package_ndc": "68382-569-05", "marketing_start_date": "20170601"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-06)", "package_ndc": "68382-569-06", "marketing_start_date": "20170601"}, {"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-10)", "package_ndc": "68382-569-10", "marketing_start_date": "20170601"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-16)", "package_ndc": "68382-569-16", "marketing_start_date": "20170601"}, {"sample": false, "description": "180 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-28)", "package_ndc": "68382-569-28", "marketing_start_date": "20170601"}], "brand_name": "acamprosate calcium", "product_id": "68382-569_2e5f04a0-3e2d-494f-837b-18570b6a8546", "dosage_form": "TABLET, DELAYED RELEASE", "product_ndc": "68382-569", "generic_name": "acamprosate calcium", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "acamprosate calcium", "active_ingredients": [{"name": "ACAMPROSATE CALCIUM", "strength": "333 mg/1"}], "application_number": "ANDA205995", "marketing_category": "ANDA", "marketing_start_date": "20170601", "listing_expiration_date": "20261231"}