procainamide hydrochloride
Generic: procainamide hydrochloride
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
procainamide hydrochloride
Generic Name
procainamide hydrochloride
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
procainamide hydrochloride 100 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
25021-322
Product ID
25021-322_65bd5a24-3fbb-4264-b26f-5839143936db
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA218135
Listing Expiration
2026-12-31
Marketing Start
2025-01-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021322
Hyphenated Format
25021-322
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
ANDA218135 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/mL
Packaging
- 10 VIAL in 1 CARTON (25021-322-10) / 10 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "65bd5a24-3fbb-4264-b26f-5839143936db", "openfda": {"unii": ["SI4064O0LX"], "rxcui": ["857886", "857962"], "spl_set_id": ["358c956e-8c6c-4bd6-a6bc-194d5b3d6d9a"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-322-10) / 10 mL in 1 VIAL", "package_ndc": "25021-322-10", "marketing_start_date": "20250115"}], "brand_name": "Procainamide Hydrochloride", "product_id": "25021-322_65bd5a24-3fbb-4264-b26f-5839143936db", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "25021-322", "generic_name": "Procainamide Hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Procainamide Hydrochloride", "active_ingredients": [{"name": "PROCAINAMIDE HYDROCHLORIDE", "strength": "100 mg/mL"}], "application_number": "ANDA218135", "marketing_category": "ANDA", "marketing_start_date": "20250115", "listing_expiration_date": "20261231"}