papaverine hydrochloride
Generic: papaverine hydrochloride
Labeler: american regent, inc.Drug Facts
Product Profile
Brand Name
papaverine hydrochloride
Generic Name
papaverine hydrochloride
Labeler
american regent, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
papaverine hydrochloride 30 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0517-4002
Product ID
0517-4002_0a4f7219-b60d-46ff-9c63-e21271569771
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
UNAPPROVED DRUG OTHER
Listing Expiration
2026-12-31
Marketing Start
1995-09-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05174002
Hyphenated Format
0517-4002
Supplemental Identifiers
RxCUI
UPC
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
papaverine hydrochloride (source: ndc)
Generic Name
papaverine hydrochloride (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/mL
Packaging
- 25 VIAL in 1 CARTON (0517-4002-25) / 2 mL in 1 VIAL (0517-4002-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0a4f7219-b60d-46ff-9c63-e21271569771", "openfda": {"upc": ["0305174002257"], "unii": ["23473EC6BQ"], "rxcui": ["1789947"], "spl_set_id": ["9e5e2ce4-7a57-4c61-a826-64c8d11d038e"], "manufacturer_name": ["American Regent, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0517-4002-25) / 2 mL in 1 VIAL (0517-4002-01)", "package_ndc": "0517-4002-25", "marketing_start_date": "19950901"}], "brand_name": "Papaverine Hydrochloride", "product_id": "0517-4002_0a4f7219-b60d-46ff-9c63-e21271569771", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0517-4002", "generic_name": "Papaverine Hydrochloride", "labeler_name": "American Regent, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Papaverine Hydrochloride", "active_ingredients": [{"name": "PAPAVERINE HYDROCHLORIDE", "strength": "30 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "19950901", "listing_expiration_date": "20261231"}