papaverine hydrochloride

Generic: papaverine hydrochloride

Labeler: nexus pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name papaverine hydrochloride
Generic Name papaverine hydrochloride
Labeler nexus pharmaceuticals, llc
Dosage Form INJECTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

papaverine hydrochloride 30 mg/mL

Manufacturer
Nexus Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 14789-121
Product ID 14789-121_28dc648b-5306-8daf-e063-6294a90a9b44
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2021-06-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 14789121
Hyphenated Format 14789-121

Supplemental Identifiers

RxCUI
1789947
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
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 30 mg/mL
source: ndc
Packaging
  • 10 VIAL, SINGLE-USE in 1 CARTON (14789-121-05) / 2 mL in 1 VIAL, SINGLE-USE (14789-121-07)
source: ndc

Packages (1)

14789-121-05 10 VIAL, SINGLE-USE in 1 CARTON (14789-121-05) / 2 mL in 1 VIAL, SINGLE-USE (14789-121-07)

Ingredients (1)

papaverine hydrochloride (30 mg/mL)

Linked Drug Pages (1)

Papaverine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "28dc648b-5306-8daf-e063-6294a90a9b44", "openfda": {"unii": ["23473EC6BQ"], "rxcui": ["1789947"], "spl_set_id": ["1e76839f-82eb-42a8-abc2-e7fbc533082d"], "manufacturer_name": ["Nexus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (14789-121-05)  / 2 mL in 1 VIAL, SINGLE-USE (14789-121-07)", "package_ndc": "14789-121-05", "marketing_start_date": "20210628"}], "brand_name": "Papaverine Hydrochloride", "product_id": "14789-121_28dc648b-5306-8daf-e063-6294a90a9b44", "dosage_form": "INJECTION", "product_ndc": "14789-121", "generic_name": "Papaverine Hydrochloride", "labeler_name": "Nexus Pharmaceuticals, LLC", "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": "20210628", "listing_expiration_date": "20261231"}