sodium bicarbonate
Generic: sodium bicarbonate
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
sodium bicarbonate
Generic Name
sodium bicarbonate
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
sodium bicarbonate 42 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0409-5555
Product ID
0409-5555_e3a44e63-8594-40b6-a3fa-d135b3149661
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202981
Listing Expiration
2027-12-31
Marketing Start
2020-08-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04095555
Hyphenated Format
0409-5555
Supplemental Identifiers
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 (source: ndc)
Application Number
ANDA202981 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 42 mg/mL
Packaging
- 25 VIAL, SINGLE-USE in 1 TRAY (0409-5555-01) / 5 mL in 1 VIAL, SINGLE-USE (0409-5555-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "e3a44e63-8594-40b6-a3fa-d135b3149661", "openfda": {"unii": ["8MDF5V39QO"], "spl_set_id": ["0c24b592-4bc8-456f-acac-9c9525844a06"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-USE in 1 TRAY (0409-5555-01) / 5 mL in 1 VIAL, SINGLE-USE (0409-5555-11)", "package_ndc": "0409-5555-01", "marketing_start_date": "20200826"}], "brand_name": "Sodium Bicarbonate", "product_id": "0409-5555_e3a44e63-8594-40b6-a3fa-d135b3149661", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "0409-5555", "generic_name": "SODIUM BICARBONATE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Bicarbonate", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "42 mg/mL"}], "application_number": "ANDA202981", "marketing_category": "ANDA", "marketing_start_date": "20200826", "listing_expiration_date": "20271231"}