antacid

Generic: calcium carbonate

Labeler: advance pharmaceutical inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH FINAL Inactive Finished

Drug Facts

Product Profile

Brand Name antacid
Generic Name calcium carbonate
Labeler advance pharmaceutical inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

calcium carbonate 648 mg/1

Manufacturer
Advance Pharmaceutical Inc.

Identifiers & Regulatory

Product NDC 17714-025
Product ID 17714-025_60f41580-e08d-faad-e053-2a91aa0a9076
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH FINAL
Application Number part331
Listing Expiration 2026-12-31
Marketing Start 1990-04-06

Pharmacologic Class

Classes
blood coagulation factor [epc] calcium [cs] cations divalent [cs] increased coagulation factor activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 17714025
Hyphenated Format 17714-025

Supplemental Identifiers

RxCUI
577040
UPC
0017714025014
UNII
H0G9379FGK

Packaging Origin

Original Packager
true

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 part331 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 648 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (17714-025-01)
  • 1000 TABLET in 1 BOTTLE (17714-025-10)
source: ndc

Packages (2)

17714-025-01 100 TABLET in 1 BOTTLE (17714-025-01) 17714-025-10 1000 TABLET in 1 BOTTLE (17714-025-10)

Ingredients (1)

calcium carbonate (648 mg/1)

Linked Drug Pages (1)

ANTACID ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "60f41580-e08d-faad-e053-2a91aa0a9076", "openfda": {"upc": ["0017714025014"], "unii": ["H0G9379FGK"], "rxcui": ["577040"], "spl_set_id": ["0108b97f-02e9-4f86-9f33-cde4f919affd"], "manufacturer_name": ["Advance Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (17714-025-01)", "package_ndc": "17714-025-01", "marketing_start_date": "19900406"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (17714-025-10)", "package_ndc": "17714-025-10", "marketing_start_date": "19900406"}], "brand_name": "ANTACID", "product_id": "17714-025_60f41580-e08d-faad-e053-2a91aa0a9076", "dosage_form": "TABLET", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]"], "product_ndc": "17714-025", "generic_name": "Calcium Carbonate", "labeler_name": "Advance Pharmaceutical Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ANTACID", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "648 mg/1"}], "application_number": "part331", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "19900406", "listing_expiration_date": "20261231"}