papaverine hydrochloride

Generic: papaverine hydrochloride

Labeler: american regent, inc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name papaverine hydrochloride
Generic Name papaverine hydrochloride
Labeler american regent, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

papaverine hydrochloride 30 mg/mL

Manufacturer
American Regent, Inc.

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
1789947
UPC
0305174002257
UNII
23473EC6BQ

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 papaverine hydrochloride (source: ndc)
Generic Name papaverine hydrochloride (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 30 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (0517-4002-25) / 2 mL in 1 VIAL (0517-4002-01)
source: ndc

Packages (1)

Ingredients (1)

papaverine hydrochloride (30 mg/mL)

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"}