quality choice ultra strength

Generic: antacid tablets (calcium carbonate)

Labeler: quality choice (chain drug marketing assoiciation)
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name quality choice ultra strength
Generic Name antacid tablets (calcium carbonate)
Labeler quality choice (chain drug marketing assoiciation)
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

calcium carbonate 1000 mg/1

Manufacturer
QUALITY CHOICE (Chain drug Marketing Assoiciation)

Identifiers & Regulatory

Product NDC 83324-317
Product ID 83324-317_451fee83-4985-b294-e063-6294a90aa788
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2024-11-11

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 83324317
Hyphenated Format 83324-317

Supplemental Identifiers

RxCUI
308892
UPC
0635515968486
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 quality choice ultra strength (source: ndc)
Generic Name antacid tablets (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 (83324-317-72)
source: ndc

Packages (1)

83324-317-72 72 TABLET, CHEWABLE in 1 BOTTLE (83324-317-72)

Ingredients (1)

calcium carbonate (1000 mg/1)

Linked Drug Pages (1)

QUALITY CHOICE Ultra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "451fee83-4985-b294-e063-6294a90aa788", "openfda": {"upc": ["0635515968486"], "unii": ["H0G9379FGK"], "rxcui": ["308892"], "spl_set_id": ["b074a885-5d10-46e4-8de9-dd9460968dad"], "manufacturer_name": ["QUALITY CHOICE (Chain drug Marketing Assoiciation)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE (83324-317-72)", "package_ndc": "83324-317-72", "marketing_start_date": "20241111"}], "brand_name": "QUALITY CHOICE Ultra Strength", "product_id": "83324-317_451fee83-4985-b294-e063-6294a90aa788", "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": "83324-317", "generic_name": "Antacid Tablets (Calcium Carbonate)", "labeler_name": "QUALITY CHOICE (Chain drug Marketing Assoiciation)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "QUALITY CHOICE", "brand_name_suffix": "Ultra Strength", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "1000 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241111", "listing_expiration_date": "20261231"}