Package 24689-137-01

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 24689-137-01
Digits Only 2468913701
Product NDC 24689-137
Product ID 24689-137_08352100-b59d-c799-e063-6294a90a5e3b
Description

1000 TABLET in 1 BOTTLE (24689-137-01)

Marketing

Marketing Status
Marketed Since 2022-06-24
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": "08352100-b59d-c799-e063-6294a90a5e3b", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["198861"], "spl_set_id": ["e206c240-55c2-2d00-e053-2a95a90a1779"], "manufacturer_name": ["APNAR PHARMA LP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (24689-137-01)", "package_ndc": "24689-137-01", "marketing_start_date": "20220624"}], "brand_name": "Sodium Bicarbonate", "product_id": "24689-137_08352100-b59d-c799-e063-6294a90a5e3b", "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": "24689-137", "generic_name": "Sodium Bicarbonate", "labeler_name": "APNAR PHARMA LP", "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": "20220624", "listing_expiration_date": "20261231"}