United States· US:43063-348_41379e71-36e8-db5a-e063-6394a90a63ae
DIETHYLPROPION HYDROCHLORIDE
A medicinal product containing diethylpropion hydrochloride, registered in United States by PD-Rx Pharmaceuticals, Inc..
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- DIETHYLPROPION HYDROCHLORIDE
- Manufacturer
- PD-Rx Pharmaceuticals, 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 · 20
- ndc1143063-348-01
- ndc1143063-348-07
- ndc1143063-348-14
- ndc1143063-348-21
- ndc1143063-348-28
- ndc1143063-348-30
- ndc1143063-348-56
- ndc1143063-348-60
- ndc1143063-348-90
- ndc1143063-348-93
- ndc114306334801100 TABLET in 1 BOTTLE, PLASTIC (43063-348-01)
- ndc1143063348077 TABLET in 1 BOTTLE, PLASTIC (43063-348-07)
- ndc11430633481414 TABLET in 1 BOTTLE, PLASTIC (43063-348-14)
- ndc11430633482121 TABLET in 1 BOTTLE, PLASTIC (43063-348-21)
- ndc11430633482828 TABLET in 1 BOTTLE, PLASTIC (43063-348-28)
- ndc11430633483030 TABLET in 1 BOTTLE, PLASTIC (43063-348-30)
- ndc11430633485656 TABLET in 1 BOTTLE, PLASTIC (43063-348-56)
- ndc11430633486060 TABLET in 1 BOTTLE, PLASTIC (43063-348-60)
- ndc11430633489090 TABLET in 1 BOTTLE, PLASTIC (43063-348-90)
- ndc114306334893180 TABLET in 1 BOTTLE, PLASTIC (43063-348-93)
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.
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/d9d12aaf-65d7-4e3b-8981-65f3c1fa7b8f GET /v1/drugs/d9d12aaf-65d7-4e3b-8981-65f3c1fa7b8f?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": "25",
"substance": "DIETHYLPROPION HYDROCHLORIDE",
"productndc": "43063-348",
"dosage_form": "TABLET",
"dea_schedule": "CIV",
"strength_unit": "mg/1",
"application_number": "ANDA201212",
"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.