Package 55681-307-02

Brand: sodium bicarbonate 5 gr

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 55681-307-02
Digits Only 5568130702
Product NDC 55681-307
Description

200 TABLET in 1 BOTTLE (55681-307-02)

Marketing

Marketing Status
Marketed Since 2022-06-30
Brand sodium bicarbonate 5 gr
Generic sodium bicarbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3906ccd8-2417-3960-e063-6394a90acc2a", "openfda": {"upc": ["0816516013775"], "unii": ["8MDF5V39QO"], "rxcui": ["198859"], "spl_set_id": ["e325d899-d9a6-5adb-e053-2995a90ac861"], "manufacturer_name": ["TWIN MED LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE (55681-307-02)", "package_ndc": "55681-307-02", "marketing_start_date": "20220630"}], "brand_name": "Sodium Bicarbonate 5 gr", "product_id": "55681-307_3906ccd8-2417-3960-e063-6394a90acc2a", "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": "55681-307", "generic_name": "Sodium Bicarbonate", "labeler_name": "TWIN MED LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sodium Bicarbonate 5 gr", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "325 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220630", "listing_expiration_date": "20261231"}