sodium bicarbonate

Generic: sodium bicarbonate

Labeler: glenmark pharmaceuticals inc., usa
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium bicarbonate
Generic Name sodium bicarbonate
Labeler glenmark pharmaceuticals inc., usa
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

sodium bicarbonate 84 mg/mL

Manufacturer
Glenmark Pharmaceuticals Inc., USA

Identifiers & Regulatory

Product NDC 68462-951
Product ID 68462-951_f38d0dfc-9bcc-4224-a202-885c9ad0beae
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA219701
Listing Expiration 2026-12-31
Marketing Start 2025-08-07

Pharmacologic Class

Classes
alkalinizing activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68462951
Hyphenated Format 68462-951

Supplemental Identifiers

RxCUI
1868486
UPC
0368462951507 0368462951651
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 ANDA219701 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 84 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (68462-951-65) / 50 mL in 1 VIAL (68462-951-50)
source: ndc

Packages (1)

68462-951-65 25 VIAL in 1 CARTON (68462-951-65) / 50 mL in 1 VIAL (68462-951-50)

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": "f38d0dfc-9bcc-4224-a202-885c9ad0beae", "openfda": {"upc": ["0368462951507", "0368462951651"], "unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["f38d0dfc-9bcc-4224-a202-885c9ad0beae"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (68462-951-65)  / 50 mL in 1 VIAL (68462-951-50)", "package_ndc": "68462-951-65", "marketing_start_date": "20250807"}], "brand_name": "SODIUM BICARBONATE", "product_id": "68462-951_f38d0dfc-9bcc-4224-a202-885c9ad0beae", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "68462-951", "generic_name": "SODIUM BICARBONATE", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM BICARBONATE", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "84 mg/mL"}], "application_number": "ANDA219701", "marketing_category": "ANDA", "marketing_start_date": "20250807", "listing_expiration_date": "20261231"}