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United States· US:64850-506_b65e0266-7172-4730-8f93-eb42e08fb7b8

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate

A medicinal product containing amphetamine aspartate monohydrate; amphetamine sulfate; dextroamphetamine saccharate; dextroamphetamine sulfate, registered in United States by Elite Laboratories, Inc..

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…normalisedDextroamphetamine Saccharate, Ampheta…ATC—REGISTER NO.US:64850-506_b65e0266…PACKS LISTED6CHECKEDJuly 19, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
AMPHETAMINE ASPARTATE MONOHYDRATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
Manufacturer
Elite Laboratories, Inc.
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
July 19, 2026

Packs & prices · 6

  • ndc11
    64850-506-05
  • ndc11
    6485050601
    100 TABLET in 1 BOTTLE (64850-506-01)
  • ndc11
    6485050605
    500 TABLET in 1 BOTTLE (64850-506-05)
  • ndc11
    6485050630
    30 TABLET in 1 BOTTLE (64850-506-30)
  • ndc11
    64850-506-30
  • ndc11
    64850-506-01

Regulatory notes

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

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/e42b386e-f22a-4e5e-a082-10ec9b066f2e
GET /v1/drugs/e42b386e-f22a-4e5e-a082-10ec9b066f2e?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": "ORAL",
  "source": "ndc",
  "strength": "7.5; 7.5; 7.5; 7.5",
  "substance": "AMPHETAMINE ASPARTATE MONOHYDRATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE",
  "productndc": "64850-506",
  "dosage_form": "TABLET",
  "dea_schedule": "CII",
  "strength_unit": "mg/1; mg/1; mg/1; mg/1",
  "application_number": "ANDA211352",
  "marketing_category": "ANDA"
}

See everything about amphetamine aspartate monohydrate; amphetamine sulfate; dextroamphetamine saccharate; dextroamphetamine sulfate.

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.