Package 50090-0530-0

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 50090-0530-0
Digits Only 5009005300
Product NDC 50090-0530
Description

50 mL in 1 VIAL (50090-0530-0)

Marketing

Marketing Status
Marketed Since 2021-03-01
Brand sodium bicarbonate
Generic sodium bicarbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b29cb3b6-4913-49b3-82a2-590b1792703a", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["619cb558-84e5-43ea-91e9-28c764f9f9c0"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 VIAL (50090-0530-0)", "package_ndc": "50090-0530-0", "marketing_start_date": "20210301"}], "brand_name": "Sodium Bicarbonate", "product_id": "50090-0530_b29cb3b6-4913-49b3-82a2-590b1792703a", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "50090-0530", "generic_name": "SODIUM BICARBONATE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Bicarbonate", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "84 mg/mL"}], "application_number": "ANDA202432", "marketing_category": "ANDA", "marketing_start_date": "20210301", "listing_expiration_date": "20261231"}