sodium bicarbonate

Generic: sodium bicarbonate

Labeler: sun pharmaceutical industries limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium bicarbonate
Generic Name sodium bicarbonate
Labeler sun pharmaceutical industries limited
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

sodium bicarbonate 84 mg/mL

Manufacturer
Sun Pharmaceutical Industries Limited

Identifiers & Regulatory

Product NDC 70095-050
Product ID 70095-050_5ae65432-04a1-4b6b-8536-2535064fc782
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217594
Listing Expiration 2026-12-31
Marketing Start 2024-03-15

Pharmacologic Class

Classes
alkalinizing activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70095050
Hyphenated Format 70095-050

Supplemental Identifiers

RxCUI
1868486
UPC
0370095050014
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 ANDA217594 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 84 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (70095-050-03) / 50 mL in 1 VIAL (70095-050-01)
source: ndc

Packages (1)

70095-050-03 25 VIAL in 1 CARTON (70095-050-03) / 50 mL in 1 VIAL (70095-050-01)

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": "5ae65432-04a1-4b6b-8536-2535064fc782", "openfda": {"upc": ["0370095050014"], "unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["5ae65432-04a1-4b6b-8536-2535064fc782"], "manufacturer_name": ["Sun Pharmaceutical Industries Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70095-050-03)  / 50 mL in 1 VIAL (70095-050-01)", "package_ndc": "70095-050-03", "marketing_start_date": "20240315"}], "brand_name": "SODIUM BICARBONATE", "product_id": "70095-050_5ae65432-04a1-4b6b-8536-2535064fc782", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "70095-050", "generic_name": "SODIUM BICARBONATE", "labeler_name": "Sun Pharmaceutical Industries Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM BICARBONATE", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "84 mg/mL"}], "application_number": "ANDA217594", "marketing_category": "ANDA", "marketing_start_date": "20240315", "listing_expiration_date": "20261231"}