Package 55681-332-10

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 55681-332-10
Digits Only 5568133210
Product NDC 55681-332
Product ID 55681-332_39a1a22c-9f3f-d168-e063-6394a90a31d6
Description

1000 TABLET in 1 BOTTLE (55681-332-10)

Marketing

Marketing Status
Marketed Since 2025-04-01
Brand sodium bicarbonate
Generic sodium bicarbonate
Sample Package No

Linked Drug Pages (1)

Sodium Bicarbonate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "39a1a22c-9f3f-d168-e063-6394a90a31d6", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["198861"], "spl_set_id": ["0f867f56-4bc0-4a85-b9d2-a16282b7c82b"], "manufacturer_name": ["TWIN MED LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (55681-332-10)", "package_ndc": "55681-332-10", "marketing_start_date": "20250401"}], "brand_name": "Sodium Bicarbonate", "product_id": "55681-332_39a1a22c-9f3f-d168-e063-6394a90a31d6", "dosage_form": "TABLET", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "55681-332", "generic_name": "Sodium Bicarbonate", "labeler_name": "TWIN MED LLC", "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": "20250401", "listing_expiration_date": "20261231"}