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United States· US:60687-921_485ceb49-adae-1b29-e063-6294a90aded8

Norethindrone Acetate

A medicinal product containing norethindrone acetate, registered in United States by American Health Packaging.

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…normalisedNorethindrone AcetateATC—REGISTER NO.US:60687-921_485ceb49…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
NORETHINDRONE ACETATE
Manufacturer
American Health Packaging
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

  • ndc11
    60687-921-21
  • ndc11
    6068792121
    30 BLISTER PACK in 1 CARTON (60687-921-21) / 1 TABLET in 1 BLISTER PACK (60687-921-11)

Regulatory notes

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

Same medicine, other countries

Norethindrone acetate in 13 other countries

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

All norethindrone acetate products

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/06f27dd3-5b76-4a0b-8177-7f83448c69b1
GET /v1/drugs/06f27dd3-5b76-4a0b-8177-7f83448c69b1?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": "5",
  "substance": "NORETHINDRONE ACETATE",
  "productndc": "60687-921",
  "dosage_form": "TABLET",
  "dea_schedule": null,
  "strength_unit": "mg/1",
  "application_number": "ANDA091090",
  "marketing_category": "ANDA"
}

See everything about norethindrone acetate.

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.