Package 21130-031-72

Brand: ultra strength

Generic: antacid tablets
NDC Package

Package Facts

Identity

Package NDC 21130-031-72
Digits Only 2113003172
Product NDC 21130-031
Product ID 21130-031_424a162b-7e6b-5083-e063-6294a90ae5af
Description

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

Marketing

Marketing Status
Marketed Since 2020-10-05
Brand ultra strength
Generic antacid tablets
Sample Package No

Linked Drug Pages (1)

Ultra Strength ndc-match (0.95)

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"}