procainamide hydrochloride

Generic: procainamide hydrochloride

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name procainamide hydrochloride
Generic Name procainamide hydrochloride
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

procainamide hydrochloride 100 mg/mL

Manufacturer
Hospira, Inc.

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
antiarrhythmic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04091902
Hyphenated Format 0409-1902

Supplemental Identifiers

RxCUI
857886
UNII
SI4064O0LX

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 procainamide hydrochloride (source: ndc)
Generic Name procainamide hydrochloride (source: ndc)
Application Number ANDA089069 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 mg/mL
source: ndc
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
source: ndc

Packages (1)

Ingredients (1)

procainamide hydrochloride (100 mg/mL)

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"}