Package 0904-7261-61

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 0904-7261-61
Digits Only 0904726161
Product NDC 0904-7261
Description

10 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-7261-61) / 10 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2022-10-26
Brand sodium bicarbonate
Generic sodium bicarbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "289e96ec-d8d1-ee93-e063-6394a90a38d7", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["198861"], "spl_set_id": ["ebf340c9-0b6d-13d2-e053-2995a90ae338"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-7261-61)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7261-61", "marketing_start_date": "20221026"}], "brand_name": "Sodium Bicarbonate", "product_id": "0904-7261_289e96ec-d8d1-ee93-e063-6394a90a38d7", "dosage_form": "TABLET", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0904-7261", "generic_name": "Sodium Bicarbonate", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sodium Bicarbonate", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "650 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221026", "listing_expiration_date": "20261231"}