Package 0280-0042-08
Brand: alka-seltzer extra strength heartburn reliefchews
Generic: calcium carbonatePackage Facts
Identity
Package NDC
0280-0042-08
Digits Only
0280004208
Product NDC
0280-0042
Description
8 TABLET, CHEWABLE in 1 POUCH (0280-0042-08)
Marketing
Marketing Status
Brand
alka-seltzer extra strength heartburn reliefchews
Generic
calcium carbonate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45261270-336f-5073-e063-6394a90acc38", "openfda": {"upc": ["0016500554592"], "unii": ["H0G9379FGK"], "rxcui": ["308915"], "spl_set_id": ["51759451-63a8-0fb4-e054-00144ff8d46c"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "8 TABLET, CHEWABLE in 1 POUCH (0280-0042-08)", "package_ndc": "0280-0042-08", "marketing_start_date": "20160915"}, {"sample": false, "description": "36 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (0280-0042-36)", "package_ndc": "0280-0042-36", "marketing_start_date": "20160915"}, {"sample": false, "description": "60 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (0280-0042-60)", "package_ndc": "0280-0042-60", "marketing_start_date": "20160915"}, {"sample": false, "description": "90 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (0280-0042-90)", "package_ndc": "0280-0042-90", "marketing_start_date": "20160915"}], "brand_name": "Alka-Seltzer Extra Strength Heartburn ReliefChews", "product_id": "0280-0042_45261270-336f-5073-e063-6394a90acc38", "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": "0280-0042", "generic_name": "Calcium carbonate", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Extra Strength Heartburn ReliefChews", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "750 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160915", "listing_expiration_date": "20261231"}