United States· US:68462-303_9240d076-c4e6-4897-af0b-a2c403a6f06d
HEATHER
A medicinal product containing norethindrone, registered in United States by Glenmark Pharmaceuticals Inc., USA.
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
- NORETHINDRONE
- Manufacturer
- Glenmark Pharmaceuticals Inc., USA
- 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 · 2
- ndc1168462303293 BLISTER PACK in 1 CARTON (68462-303-29) / 28 TABLET in 1 BLISTER PACK (68462-303-84)
- ndc1168462-303-29
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Norethindrone in 13 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FinlandMini-PillOrifarm Oy
- United KingdomMicronor 350microgram tabletsJanssen-Cilag Ltd
- CanadaJENCYCLALUPIN PHARMA CANADA LIMITED
- IrelandNoriday 350 micrograms tabletsPCO Manufacturing Ltd.
- NorwayConludagPfizer AS
- SwedenMini-Pe 0,35 mg TablettPfizer AB
- PolandPrimolut-NorBayer AG
- BelgiumActivelle 1 mg - 0.5 mgImpexeco
Authorised across Europe · EMA
The same active substance is authorised in 18 EEA countries. Names it is sold under:
- Bulgaria · Примолут-Нор
- Cyprus · Norethisterone Remedica
- Czechia · Norethisteron Zentiva
- Denmark · Mini-Pe
- Spain · Primolut-Nor
- Finland · Mini-Pill, Primolut N
- United Kingdom (Northern Ireland) · Norethisterone Noumed Life Sciences, Norethisterone Wockhardt Uk
- Hungary · Norcolut
- Ireland · Noriday
- Iceland · Primolut N
- Italy · Primolut Nor
- Malta · Norethisterone Remedica
- Netherlands · Primolut N
- Norway · Conludag, Primolut N
- Poland · Primolut-Nor
- Sweden · Mini-Pe, Primolut-Nor
- Slovenia · Primolut Nor
- Slovakia · Norethisteron Zentiva
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/2acad600-1703-4344-95e1-f91d3fce6bc2 GET /v1/drugs/2acad600-1703-4344-95e1-f91d3fce6bc2?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": ".35",
"substance": "NORETHINDRONE",
"productndc": "68462-303",
"dosage_form": "TABLET",
"dea_schedule": null,
"strength_unit": "mg/1",
"application_number": "ANDA090454",
"marketing_category": "ANDA"
}See everything about norethindrone.
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.