antacid
Generic: calcium carbonate
Labeler: meijer distribution incDrug Facts
Product Profile
Brand Name
antacid
Generic Name
calcium carbonate
Labeler
meijer distribution inc
Dosage Form
TABLET, CHEWABLE
Routes
Active Ingredients
calcium carbonate 750 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
41250-553
Product ID
41250-553_41e4d104-a8cb-e3a6-e063-6294a90af0fe
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M001
Listing Expiration
2026-12-31
Marketing Start
2017-03-14
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
41250553
Hyphenated Format
41250-553
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
antacid (source: ndc)
Generic Name
calcium carbonate (source: ndc)
Application Number
M001 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 750 mg/1
Packaging
- 200 TABLET, CHEWABLE in 1 BOTTLE (41250-553-20)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41e4d104-a8cb-e3a6-e063-6294a90af0fe", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["308915"], "spl_set_id": ["9b0d3f90-54aa-4256-8e06-466655407e13"], "manufacturer_name": ["Meijer Distribution Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET, CHEWABLE in 1 BOTTLE (41250-553-20)", "package_ndc": "41250-553-20", "marketing_start_date": "20170314"}], "brand_name": "Antacid", "product_id": "41250-553_41e4d104-a8cb-e3a6-e063-6294a90af0fe", "dosage_form": "TABLET, CHEWABLE", "product_ndc": "41250-553", "generic_name": "Calcium carbonate", "labeler_name": "Meijer Distribution Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Antacid", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "750 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170314", "listing_expiration_date": "20261231"}