ultra strength antacid

Generic: antacid

Labeler: target corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name ultra strength antacid
Generic Name antacid
Labeler target corporation
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

calcium carbonate 1000 mg/1

Manufacturer
Target Corporation

Identifiers & Regulatory

Product NDC 11673-933
Product ID 11673-933_42c23ba3-b826-b876-e063-6394a90a1795
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2018-01-05

Pharmacologic Class

Classes
blood coagulation factor [epc] calcium [cs] cations divalent [cs] increased coagulation factor activity [pe] phosphate binder [epc] phosphate chelating activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673933
Hyphenated Format 11673-933

Supplemental Identifiers

RxCUI
308892
UPC
0492450504199
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 ultra strength antacid (source: ndc)
Generic Name antacid (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (11673-933-72)
source: ndc

Packages (1)

11673-933-72 72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (11673-933-72)

Ingredients (1)

calcium carbonate (1000 mg/1)

Linked Drug Pages (1)

ultra strength antacid ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "42c23ba3-b826-b876-e063-6394a90a1795", "openfda": {"upc": ["0492450504199"], "unii": ["H0G9379FGK"], "rxcui": ["308892"], "spl_set_id": ["2125e81b-23c6-4c5f-a6aa-829f8d3df71f"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (11673-933-72)", "package_ndc": "11673-933-72", "marketing_start_date": "20180105"}], "brand_name": "ultra strength antacid", "product_id": "11673-933_42c23ba3-b826-b876-e063-6394a90a1795", "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": "11673-933", "generic_name": "Antacid", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ultra strength antacid", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "1000 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180105", "listing_expiration_date": "20261231"}