procainamide hydrochloride
Generic: procainamide hydrochloride
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
procainamide hydrochloride
Generic Name
procainamide hydrochloride
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
procainamide hydrochloride 100 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0409-1902
Product ID
0409-1902_5c75003d-8b7f-4e26-b76e-11a749a53ae6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA089069
Listing Expiration
2027-12-31
Marketing Start
2006-03-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04091902
Hyphenated Format
0409-1902
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
procainamide hydrochloride (source: ndc)
Generic Name
procainamide hydrochloride (source: ndc)
Application Number
ANDA089069 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/mL
Packaging
- 25 CARTON in 1 CASE (0409-1902-01) / 1 VIAL, MULTI-DOSE in 1 CARTON (0409-1902-11) / 10 mL in 1 VIAL, MULTI-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "5c75003d-8b7f-4e26-b76e-11a749a53ae6", "openfda": {"unii": ["SI4064O0LX"], "rxcui": ["857886"], "spl_set_id": ["17e47845-daad-434c-a784-6d3875b0d704"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 CARTON in 1 CASE (0409-1902-01) / 1 VIAL, MULTI-DOSE in 1 CARTON (0409-1902-11) / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "0409-1902-01", "marketing_start_date": "20060308"}], "brand_name": "Procainamide Hydrochloride", "product_id": "0409-1902_5c75003d-8b7f-4e26-b76e-11a749a53ae6", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "0409-1902", "generic_name": "PROCAINAMIDE HYDROCHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Procainamide Hydrochloride", "active_ingredients": [{"name": "PROCAINAMIDE HYDROCHLORIDE", "strength": "100 mg/mL"}], "application_number": "ANDA089069", "marketing_category": "ANDA", "marketing_start_date": "20060308", "listing_expiration_date": "20271231"}