sodium bicarbonate
Generic: sodium bicarbonate
Labeler: civicaDrug Facts
Product Profile
Brand Name
sodium bicarbonate
Generic Name
sodium bicarbonate
Labeler
civica
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
sodium bicarbonate 84 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72572-740
Product ID
72572-740_8fcbd37e-e4d5-4137-9abf-c398fbb5cbf0
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
72572740
Hyphenated Format
72572-740
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
- 25 VIAL in 1 CARTON (72572-740-25) / 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": "8fcbd37e-e4d5-4137-9abf-c398fbb5cbf0", "openfda": {"upc": ["0372572740258"], "unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["a10fdfbc-94a0-49ab-b26c-de1df042bc89"], "manufacturer_name": ["Civica"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (72572-740-25) / 50 mL in 1 VIAL", "package_ndc": "72572-740-25", "marketing_start_date": "20240201"}], "brand_name": "Sodium Bicarbonate", "product_id": "72572-740_8fcbd37e-e4d5-4137-9abf-c398fbb5cbf0", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "72572-740", "generic_name": "SODIUM BICARBONATE", "labeler_name": "Civica", "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"}