sodium bicarbonate
Generic: sodium bicarbonate injection,
Labeler: long grove pharmaceuticals, llcDrug Facts
Product Profile
Brand Name
sodium bicarbonate
Generic Name
sodium bicarbonate injection,
Labeler
long grove pharmaceuticals, llc
Dosage Form
SOLUTION
Routes
Active Ingredients
sodium bicarbonate 84 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
81298-7620
Product ID
81298-7620_1a255946-a137-4e13-8203-65dd80b34872
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216042
Listing Expiration
2026-12-31
Marketing Start
2024-09-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
812987620
Hyphenated Format
81298-7620
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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 injection, (source: ndc)
Application Number
ANDA216042 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 84 mg/mL
Packaging
- 20 VIAL in 1 CARTON (81298-7620-3) / 50 mL in 1 VIAL (81298-7620-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "1a255946-a137-4e13-8203-65dd80b34872", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["a26d709b-b294-4b02-9a88-7e840f099a33"], "manufacturer_name": ["Long Grove Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 VIAL in 1 CARTON (81298-7620-3) / 50 mL in 1 VIAL (81298-7620-1)", "package_ndc": "81298-7620-3", "marketing_start_date": "20240930"}], "brand_name": "SODIUM BICARBONATE", "product_id": "81298-7620_1a255946-a137-4e13-8203-65dd80b34872", "dosage_form": "SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "81298-7620", "generic_name": "sodium bicarbonate injection,", "labeler_name": "Long Grove Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM BICARBONATE", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "84 mg/mL"}], "application_number": "ANDA216042", "marketing_category": "ANDA", "marketing_start_date": "20240930", "listing_expiration_date": "20261231"}