sodium bicarbonate

Generic: sodium bicarbonate

Labeler: propharma distribution
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium bicarbonate
Generic Name sodium bicarbonate
Labeler propharma distribution
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

sodium bicarbonate 84 mg/mL

Manufacturer
ProPharma Distribution

Identifiers & Regulatory

Product NDC 84549-352
Product ID 84549-352_3d71b046-3e0c-054a-e063-6294a90a563a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203449
Listing Expiration 2026-12-31
Marketing Start 2000-06-01

Pharmacologic Class

Classes
alkalinizing activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 84549352
Hyphenated Format 84549-352

Supplemental Identifiers

RxCUI
792582
UNII
8MDF5V39QO

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 ANDA203449 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 84 mg/mL
source: ndc
Packaging
  • 50 mL in 1 SYRINGE (84549-352-01)
source: ndc

Packages (1)

84549-352-01 50 mL in 1 SYRINGE (84549-352-01)

Ingredients (1)

sodium bicarbonate (84 mg/mL)

Linked Drug Pages (1)

Sodium Bicarbonate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "3d71b046-3e0c-054a-e063-6294a90a563a", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["792582"], "spl_set_id": ["3d71b046-3e0b-054a-e063-6294a90a563a"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 SYRINGE (84549-352-01)", "package_ndc": "84549-352-01", "marketing_start_date": "20250901"}], "brand_name": "Sodium Bicarbonate", "product_id": "84549-352_3d71b046-3e0c-054a-e063-6294a90a563a", "dosage_form": "INJECTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "84549-352", "generic_name": "Sodium Bicarbonate", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Bicarbonate", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "84 mg/mL"}], "application_number": "ANDA203449", "marketing_category": "ANDA", "marketing_start_date": "20000601", "listing_expiration_date": "20261231"}