sodium bicarbonate

Generic: sodium bicarbonate

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium bicarbonate
Generic Name sodium bicarbonate
Labeler northstar rx llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

sodium bicarbonate 84 mg/mL

Manufacturer
NORTHSTAR RX LLC

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
alkalinizing activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72603209
Hyphenated Format 72603-209

Supplemental Identifiers

RxCUI
1868486
UNII
8MDF5V39QO

Packaging Origin

Original Packager
true

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
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 84 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (72603-209-25) / 50 mL in 1 VIAL (72603-209-01)
source: ndc

Packages (1)

Ingredients (1)

sodium bicarbonate (84 mg/mL)

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"}