United States· US:37662-1612_e98d5ff1-ec13-5ad7-e053-2a95a90ad6d0
Thea Sinensis
A medicinal product containing green tea leaf, registered in United States by Hahnemann Laboratories, 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
- GREEN TEA LEAF
- Manufacturer
- Hahnemann 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
- September 27, 2026
Packs & prices · 8
- ndc1137662-1612-1
- ndc1137662-1612-2
- ndc1137662-1612-3
- ndc1137662-1612-4
- ndc113766216121200 PELLET in 1 VIAL, GLASS (37662-1612-1)
- ndc113766216122500 PELLET in 1 VIAL, GLASS (37662-1612-2)
- ndc1137662161233000 PELLET in 1 BOTTLE, GLASS (37662-1612-3)
- ndc11376621612410000 PELLET in 1 BOTTLE, GLASS (37662-1612-4)
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Green tea leaf in 4 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaVEREGENNORDIC Pharma, s.r.o., Jesenice u Prahy
- SwitzerlandVeregen 10%, SalbeViatris Pharma GmbH
- GermanyVeregenAresus Pharma Gmbh
- PolandVeregenORNYX OÜ
Authorised across Europe · EMA
The same active substance is authorised in 10 EEA countries. Names it is sold under:
- Austria · Veregen
- Cyprus · Veregreen
- Germany · Veregen
- Spain · Veregen
- United Kingdom (Northern Ireland) · Catephen
- Greece · Veregreen
- Ireland · Catephen
- Portugal · Veregen
- Romania · Veregen
- Slovenia · Veregen
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/d1c515e2-8841-41e3-b5a7-c83b6ceaa98f GET /v1/drugs/d1c515e2-8841-41e3-b5a7-c83b6ceaa98f?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": "1",
"substance": "GREEN TEA LEAF",
"productndc": "37662-1612",
"dosage_form": "PELLET",
"dea_schedule": null,
"strength_unit": "[hp_M]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC"
}See everything about green tea leaf.
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.