ultra strength

Generic: antacid tablets

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

Drug Facts

Product Profile

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

calcium carbonate 1000 mg/1

Manufacturer
SAFEWAY

Identifiers & Regulatory

Product NDC 21130-031
Product ID 21130-031_424a162b-7e6b-5083-e063-6294a90ae5af
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2020-10-05

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 21130031
Hyphenated Format 21130-031

Supplemental Identifiers

RxCUI
308892
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 (source: ndc)
Generic Name antacid tablets (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 (21130-031-72)
source: ndc

Packages (1)

21130-031-72 72 TABLET, CHEWABLE in 1 BOTTLE (21130-031-72)

Ingredients (1)

calcium carbonate (1000 mg/1)

Linked Drug Pages (1)

Ultra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "424a162b-7e6b-5083-e063-6294a90ae5af", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["308892"], "spl_set_id": ["4c6cdd81-5145-4a1f-888f-85cf5d856c39"], "manufacturer_name": ["SAFEWAY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE (21130-031-72)", "package_ndc": "21130-031-72", "marketing_start_date": "20201005"}], "brand_name": "Ultra Strength", "product_id": "21130-031_424a162b-7e6b-5083-e063-6294a90ae5af", "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": "21130-031", "generic_name": "Antacid Tablets", "labeler_name": "SAFEWAY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ultra Strength", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "1000 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20201005", "listing_expiration_date": "20261231"}