antacid
Generic: calcium carbonate
Labeler: advance pharmaceutical inc.Drug Facts
Product Profile
Brand Name
antacid
Generic Name
calcium carbonate
Labeler
advance pharmaceutical inc.
Dosage Form
TABLET, CHEWABLE
Routes
Active Ingredients
calcium carbonate 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
17714-041
Product ID
17714-041_2a327df7-e74f-8130-e063-6294a90a6e83
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M001
Listing Expiration
2026-12-31
Marketing Start
2007-11-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
17714041
Hyphenated Format
17714-041
Supplemental Identifiers
RxCUI
UPC
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
- 500 mg/1
Packaging
- 100 TABLET, CHEWABLE in 1 BOTTLE (17714-041-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a327df7-e74f-8130-e063-6294a90a6e83", "openfda": {"upc": ["0017714041014"], "unii": ["H0G9379FGK"], "rxcui": ["308907"], "spl_set_id": ["3203dfc5-2cb1-4703-8d81-63fba07ddd98"], "manufacturer_name": ["Advance Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, CHEWABLE in 1 BOTTLE (17714-041-01)", "package_ndc": "17714-041-01", "marketing_start_date": "20071130"}], "brand_name": "ANTACID", "product_id": "17714-041_2a327df7-e74f-8130-e063-6294a90a6e83", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "17714-041", "generic_name": "Calcium Carbonate", "labeler_name": "Advance Pharmaceutical Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ANTACID", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "500 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20071130", "listing_expiration_date": "20261231"}