sodium bicarbonate
Generic: sodium bicarbonate
Labeler: international medication systems, limitedDrug Facts
Product Profile
Brand Name
sodium bicarbonate
Generic Name
sodium bicarbonate
Labeler
international medication systems, limited
Dosage Form
INJECTION
Routes
Active Ingredients
sodium bicarbonate 84 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
76329-3352
Product ID
76329-3352_74a86dc7-0929-40d0-9661-9f9063a8fd7d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203449
Listing Expiration
2026-12-31
Marketing Start
2000-06-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
763293352
Hyphenated Format
76329-3352
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 (source: ndc)
Application Number
ANDA203449 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 84 mg/mL
Packaging
- 1 SYRINGE in 1 CARTON (76329-3352-1) / 50 mL in 1 SYRINGE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "74a86dc7-0929-40d0-9661-9f9063a8fd7d", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["792582"], "spl_set_id": ["77698221-a01d-4568-a7bc-d3d4e982875d"], "manufacturer_name": ["International Medication Systems, Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE in 1 CARTON (76329-3352-1) / 50 mL in 1 SYRINGE", "package_ndc": "76329-3352-1", "marketing_start_date": "20000601"}], "brand_name": "Sodium Bicarbonate", "product_id": "76329-3352_74a86dc7-0929-40d0-9661-9f9063a8fd7d", "dosage_form": "INJECTION", "product_ndc": "76329-3352", "generic_name": "Sodium Bicarbonate", "labeler_name": "International Medication Systems, Limited", "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": "20000601", "listing_expiration_date": "20261231"}