sodium bicarbonate
Generic: sodium bicarbonate
Labeler: northstar rx llcDrug Facts
Product Profile
Brand Name
sodium bicarbonate
Generic Name
sodium bicarbonate
Labeler
northstar rx llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
sodium bicarbonate 84 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72603-209
Product ID
72603-209_f2190c6c-50b8-4283-b715-1eabb7e4ff0f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216364
Marketing Start
2024-02-19
Marketing End
2026-06-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72603209
Hyphenated Format
72603-209
Supplemental Identifiers
RxCUI
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
ANDA216364 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 84 mg/mL
Packaging
- 25 VIAL in 1 CARTON (72603-209-25) / 50 mL in 1 VIAL (72603-209-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f2190c6c-50b8-4283-b715-1eabb7e4ff0f", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["068db1fe-0346-48f1-8d2f-8488d7331106"], "manufacturer_name": ["NORTHSTAR RX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (72603-209-25) / 50 mL in 1 VIAL (72603-209-01)", "package_ndc": "72603-209-25", "marketing_end_date": "20260630", "marketing_start_date": "20240219"}], "brand_name": "Sodium Bicarbonate", "product_id": "72603-209_f2190c6c-50b8-4283-b715-1eabb7e4ff0f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "72603-209", "generic_name": "SODIUM BICARBONATE", "labeler_name": "NORTHSTAR RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Bicarbonate", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "84 mg/mL"}], "application_number": "ANDA216364", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20240219"}