United States· US:0517-0799_94369498-af74-44d3-a7f2-0f138d140d48

Betamethasone Sodium Phosphate and Betamethasone Acetate

A medicinal product containing betamethasone acetate; betamethasone sodium phosphate, registered in United States by American Regent, Inc..

US label

Checked against FDA National Drug Code directory (United States) on September 27, 2026

Informational only — not a medical device.

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The record

At a glance

FDA National Drug Code directory (United States)

Active substance: BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE
Manufacturer: American Regent, Inc.
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
0517079901
1 VIAL, MULTI-DOSE in 1 CARTON (0517-0799-01) / 5 mL in 1 VIAL, MULTI-DOSE
ndc11
0517-0799-01

Regulatory notes

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

Same medicine, other countries

Betamethasone acetate; betamethasone sodium phosphate in 5 other countries

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

All betamethasone acetate; betamethasone sodium phosphate products

Authorised across Europe · EMA

The same active substance is authorised in 19 EEA countries. Names it is sold under:

Austria · Celestan Biphase, Diprophos
Belgium · Celestone Chronodose, Diprophos Ampoule
Bulgaria · Дипрофос
Germany · Celestan Depot, Diprosone Depot 1 Ml Ampulle
Denmark · Diprospan
Spain · Celestone Cronodose
Finland · Celeston Chronodose
France · Celestene Chronodose, Diprostene
Greece · Celestone Chronodose, Propiochrone
Hungary · Diprophos
Iceland · Diprospan
Luxembourg · Celestone Chronodose, Diprophos Ampoule
Netherlands · Celestone Chronodose
Norway · Celeston Chronodose
Poland · Diprophos
Portugal · Diprofos Depot
Romania · Diprophos
Sweden · Celeston Bifas
Slovakia · Diprophos

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/f2520a9a-d8d3-48b1-b78d-79efeddc9d6f
GET /v1/drugs/f2520a9a-d8d3-48b1-b78d-79efeddc9d6f?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": "INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR",
  "source": "ndc",
  "strength": "3; 3",
  "substance": "BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE",
  "productndc": "0517-0799",
  "dosage_form": "INJECTION, SUSPENSION",
  "dea_schedule": null,
  "strength_unit": "mg/mL; mg/mL",
  "application_number": "ANDA090747",
  "marketing_category": "ANDA"
}

API reference MCP server Plans

See everything about betamethasone acetate; betamethasone sodium phosphate.

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.

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