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United States· US:71335-0049_c150ef3f-41d3-445b-b566-4d672759a1d7

Diethylpropion Hydrochloride

A medicinal product containing diethylpropion hydrochloride, registered in United States by Bryant Ranch Prepack.

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…normalisedDiethylpropion HydrochlorideATC—REGISTER NO.US:71335-0049_c150ef3…PACKS LISTED18CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
DIETHYLPROPION HYDROCHLORIDE
Manufacturer
Bryant Ranch Prepack
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 · 18

  • ndc11
    7133500491
    30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-1)
  • ndc11
    7133500492
    28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-2)
  • ndc11
    7133500493
    90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-3)
  • ndc11
    7133500494
    7 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-4)
  • ndc11
    7133500495
    14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-5)
  • ndc11
    7133500496
    84 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-6)
  • ndc11
    7133500497
    21 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-7)
  • ndc11
    7133500498
    60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-8)
  • ndc11
    7133500499
    45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-9)
  • ndc11
    71335-0049-1
  • ndc11
    71335-0049-2
  • ndc11
    71335-0049-3
  • ndc11
    71335-0049-4
  • ndc11
    71335-0049-5
  • ndc11
    71335-0049-6
  • ndc11
    71335-0049-7
  • ndc11
    71335-0049-8
  • ndc11
    71335-0049-9

Regulatory notes

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

Same medicine, other countries

Diethylpropion hydrochloride in 1 other country

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

All diethylpropion hydrochloride products

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/0740726e-2de5-4f06-8862-4cc1ed98b5b5
GET /v1/drugs/0740726e-2de5-4f06-8862-4cc1ed98b5b5?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": "75",
  "substance": "DIETHYLPROPION HYDROCHLORIDE",
  "productndc": "71335-0049",
  "dosage_form": "TABLET, EXTENDED RELEASE",
  "dea_schedule": "CIV",
  "strength_unit": "mg/1",
  "application_number": "ANDA091680",
  "marketing_category": "ANDA"
}

See everything about diethylpropion 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.