Package 0280-4100-63

Brand: alka-seltzer gold

Generic: alka-seltzer gold
NDC Package

Package Facts

Identity

Package NDC 0280-4100-63
Digits Only 0280410063
Product NDC 0280-4100
Description

18 POUCH in 1 CARTON (0280-4100-63) / 2 TABLET, EFFERVESCENT in 1 POUCH

Marketing

Marketing Status
Marketed Since 2014-11-19
Brand alka-seltzer gold
Generic alka-seltzer gold
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4526b3d0-3667-afe5-e063-6294a90af3ab", "openfda": {"upc": ["0016500041085"], "unii": ["2968PHW8QP", "HM5Z15LEBN", "8MDF5V39QO"], "rxcui": ["1536474"], "spl_set_id": ["0824bedb-413b-2fa0-e054-00144ff88e88"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "18 POUCH in 1 CARTON (0280-4100-63)  / 2 TABLET, EFFERVESCENT in 1 POUCH", "package_ndc": "0280-4100-63", "marketing_start_date": "20141119"}], "brand_name": "Alka-Seltzer Gold", "product_id": "0280-4100_4526b3d0-3667-afe5-e063-6294a90af3ab", "dosage_form": "TABLET, EFFERVESCENT", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]", "Increased Large Intestinal Motility [PE]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "0280-4100", "generic_name": "Alka-Seltzer Gold", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Gold", "active_ingredients": [{"name": "CITRIC ACID MONOHYDRATE", "strength": "1000 mg/1"}, {"name": "POTASSIUM BICARBONATE", "strength": "344 mg/1"}, {"name": "SODIUM BICARBONATE", "strength": "1050 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20141119", "listing_expiration_date": "20261231"}