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United States· US:14789-121_28dc648b-5306-8daf-e063-6294a90a9b44

Papaverine Hydrochloride

A medicinal product containing papaverine hydrochloride, registered in United States by Nexus Pharmaceuticals, LLC.

US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedPapaverine HydrochlorideATC—REGISTER NO.US:14789-121_28dc648b…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
PAPAVERINE HYDROCHLORIDE
Manufacturer
Nexus Pharmaceuticals, LLC
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 2

  • ndc11
    1478912105
    10 VIAL, SINGLE-USE in 1 CARTON (14789-121-05) / 2 mL in 1 VIAL, SINGLE-USE (14789-121-07)
  • ndc11
    14789-121-05

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Papaverine hydrochloride in 8 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All papaverine hydrochloride products

Authorised across Europe · EMA

The same active substance is authorised in 10 EEA countries. Names it is sold under:

  • Belgium · Papaverine Hcl Sterop
  • Bulgaria · Папаверин Актавис, Папаверин Софарма
  • Germany · Paveron N
  • Denmark · Papaverin Oba
  • France · Papaverine Renaudin
  • Italy · Papaverina Cloridrato Galenica Senese, Papaverina Cloridrato Monico
  • Latvia · Papaverine Sopharma
  • Poland · Papaverinum Hydrochloricum Wzf
  • Portugal · Papaverina Labesfal
  • Romania · Papaverina, Papaverină Arena

Source: European Medicines Agency, Article 57 product data.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/99ee7c7e-24d0-47b4-a082-3f31c3cc38b0
GET /v1/drugs/99ee7c7e-24d0-47b4-a082-3f31c3cc38b0?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "route": "INTRAMUSCULAR; INTRAVENOUS",
  "source": "ndc",
  "strength": "30",
  "substance": "PAPAVERINE HYDROCHLORIDE",
  "productndc": "14789-121",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "strength_unit": "mg/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER"
}

See everything about papaverine hydrochloride.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.