ultra strength antacid

Generic: calcium carbonate

Labeler: cvs
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name ultra strength antacid
Generic Name calcium carbonate
Labeler cvs
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

calcium carbonate 1000 mg/1

Manufacturer
CVS

Identifiers & Regulatory

Product NDC 51316-171
Product ID 51316-171_35954e1d-479d-448b-97f3-d9b74c51a9ab
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2025-01-23

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 51316171
Hyphenated Format 51316-171

Supplemental Identifiers

RxCUI
308892
UPC
0050428380710
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 calcium carbonate (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 (51316-171-68)
source: ndc

Packages (1)

51316-171-68 72 TABLET, CHEWABLE in 1 BOTTLE (51316-171-68)

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": "35954e1d-479d-448b-97f3-d9b74c51a9ab", "openfda": {"upc": ["0050428380710"], "unii": ["H0G9379FGK"], "rxcui": ["308892"], "spl_set_id": ["2bc4c71c-a9c5-17df-e063-6294a90ac88c"], "manufacturer_name": ["CVS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE (51316-171-68)", "package_ndc": "51316-171-68", "marketing_start_date": "20250123"}], "brand_name": "Ultra Strength Antacid", "product_id": "51316-171_35954e1d-479d-448b-97f3-d9b74c51a9ab", "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": "51316-171", "generic_name": "Calcium carbonate", "labeler_name": "CVS", "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": "20250123", "listing_expiration_date": "20261231"}