United States· US:0904-7302_e217e8bc-db78-4d8b-beb7-3a370d14f9db
Aprodine
A medicinal product containing pseudoephedrine hydrochloride; triprolidine hydrochloride, registered in United States by Major Pharmaceuticals.
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
- PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE
- Manufacturer
- Major Pharmaceuticals
- 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 · 4
- ndc110904-7302-60
- ndc1109047302241 BLISTER PACK in 1 CARTON (0904-7302-24) / 24 TABLET, FILM COATED in 1 BLISTER PACK
- ndc1109047302601 BOTTLE, PLASTIC in 1 CARTON (0904-7302-60) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
- ndc110904-7302-24
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Pseudoephedrine hydrochloride; triprolidine hydrochloride in 4 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomMulti-Action Actifed 60mg/2.5mg tabletsMcNeil Products Ltd
- GermanyRhinopront Kombi TablettenRecordati Pharma Gmbh
- IrelandACTIFED 30 mg/1.25 mg per 5 ml SyrupJNTL Consumer Health I (Ireland) Limited
- PolandAcatar Acti-TabsUS Pharmacia Sp. z o.o.
Authorised across Europe · EMA
The same active substance is authorised in 12 EEA countries. Names it is sold under:
- Cyprus · Medofed
- Germany · Rhinopront Kombi Tabletten
- Estonia · Actifed
- United Kingdom (Northern Ireland) · Multi-Action Actifed
- Ireland · Actifed
- Italy · Actifed
- Lithuania · Actifed
- Latvia · Actifed
- Malta · Medofed
- Poland · Acatar Acti-Tabs
- Portugal · Actifed, Dinaxil
- Slovakia · Trifed
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/2392ed54-d978-4893-afa1-e4230c7cf372 GET /v1/drugs/2392ed54-d978-4893-afa1-e4230c7cf372?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": "60; 2.5",
"substance": "PSEUDOEPHEDRINE HYDROCHLORIDE; TRIPROLIDINE HYDROCHLORIDE",
"productndc": "0904-7302",
"dosage_form": "TABLET, FILM COATED",
"dea_schedule": null,
"strength_unit": "mg/1; mg/1",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG"
}See everything about pseudoephedrine hydrochloride; triprolidine 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.