sodium bicarbonate

Generic: sodium bicarbonate

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium bicarbonate
Generic Name sodium bicarbonate
Labeler remedyrepack inc.
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

sodium bicarbonate 84 mg/mL

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4158
Product ID 70518-4158_3fb730ba-82fd-149f-e063-6394a90afa94
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203449
Listing Expiration 2026-12-31
Marketing Start 2024-08-14

Pharmacologic Class

Classes
alkalinizing activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184158
Hyphenated Format 70518-4158

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
  • 1 SYRINGE in 1 CARTON (70518-4158-0) / 50 mL in 1 SYRINGE
source: ndc

Packages (1)

70518-4158-0 1 SYRINGE in 1 CARTON (70518-4158-0) / 50 mL in 1 SYRINGE

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": "3fb730ba-82fd-149f-e063-6394a90afa94", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["792582"], "spl_set_id": ["96093b76-5d98-4d2b-b851-20207a8864db"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE in 1 CARTON (70518-4158-0)  / 50 mL in 1 SYRINGE", "package_ndc": "70518-4158-0", "marketing_start_date": "20240814"}], "brand_name": "Sodium Bicarbonate", "product_id": "70518-4158_3fb730ba-82fd-149f-e063-6394a90afa94", "dosage_form": "INJECTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "70518-4158", "generic_name": "Sodium Bicarbonate", "labeler_name": "REMEDYREPACK INC.", "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": "20240814", "listing_expiration_date": "20261231"}