sodium bicarbonate
Generic: sodium bicarbonate
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
sodium bicarbonate
Generic Name
sodium bicarbonate
Labeler
a-s medication solutions
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
sodium bicarbonate 84 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6813
Product ID
50090-6813_132e1b7b-c63c-43d3-ac31-8ca034f1210f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211091
Listing Expiration
2026-12-31
Marketing Start
2019-08-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906813
Hyphenated Format
50090-6813
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
sodium bicarbonate (source: ndc)
Generic Name
sodium bicarbonate (source: ndc)
Application Number
ANDA211091 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 84 mg/mL
Packaging
- 1 VIAL in 1 CARTON (50090-6813-0) / 50 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "132e1b7b-c63c-43d3-ac31-8ca034f1210f", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["d89406d3-4356-4a8c-acc1-89efe1d27010"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (50090-6813-0) / 50 mL in 1 VIAL", "package_ndc": "50090-6813-0", "marketing_start_date": "20231108"}], "brand_name": "Sodium Bicarbonate", "product_id": "50090-6813_132e1b7b-c63c-43d3-ac31-8ca034f1210f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "50090-6813", "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": "ANDA211091", "marketing_category": "ANDA", "marketing_start_date": "20190801", "listing_expiration_date": "20261231"}