Ferring Pharmaceuticals Inc.
NDC labeler code: 55566
What is a labeler?
The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.
Official FDA data only
Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.
Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.
Prescription medicines
- Desmopressin acetateDdavp, Stimate, Desmoda · 5 products
- DinoprostoneCervidil, Prepidil · 1 product
- Ganirelix acetateFyremadel · 1 product
- ProgesteroneCrinone, Prometrium, Endometrin · 1 product
- Nadofaragene firadenovec-vncgAdstiladrin · 1 product
- Sodium picosulfate, magnesium oxide, and anhydrous citric acidClenpiq · 1 product
- Donor human stoolRebyota · 1 product
FDA applications for these products
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
- BLA: Biologics License Application: how a biologic medicine (made from living cells) is approved.
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| November 30, 2018 | ANDA204246 | Ganirelix acetate FYREMADEL | Sun Pharm |
| November 28, 2017 | NDA209589 | Sodium picosulfate, magnesium oxide, and anhydrous citric acid CLENPIQ | Ferring Pharms Inc |
| June 21, 2007 | NDA022057 | Progesterone ENDOMETRIN | Ferring |
| September 6, 1995 | NDA019955 | Desmopressin acetate DDAVP | Ferring Pharms Inc |
| March 30, 1995 | NDA020411 | Dinoprostone CERVIDIL | Ferring Pharms Inc |
| March 7, 1994 | NDA020355 | Desmopressin acetate STIMATE, STIMATE (NEEDS NO REFRIGERATION) | Ferring Pharms Inc |
| March 30, 1984 | NDA018938 | Desmopressin acetate DDAVP | J Molner |
| — | BLA125700 | Nadofaragene firadenovec-vncg | — |
| — | BLA125739 | Donor human stool | — |
The sponsor is the company that holds the FDA application; it can differ from the labeler.
Recall timeline
2023
-
April 19, 2023 · Class II · Terminated · D-0569-2023 · Ganirelix acetate
Presence of Particulate Matter: A piece of glass was found in a prefilled syringe.
Fyremadel (ganirelix acetate) injection, 250 mcg/0.5 mL, One Single Dose Sterile Prefilled Syringe 0.5 mL, For Subcutaneous Use, Rx Only, Sterile, Distributor: Ferring Pharmaceuticals Inc., Parsippany, NJ 07054, USA, NDC
2013
-
September 19, 2013 · Class III · Terminated · D-1426-2014 · Progesterone
Discoloration; due to prolonged heat exposure.
ENDOMETRIN (progesterone) Vaginal Insert 100 mg USP, 21 inserts, Rx Only, Manufactured for: Ferring Pharmaceuticals Inc. Parsippany, NJ 07054 ---- NDC 55566-6500-3
What do the recall classes mean?
Class I: The most serious type: there is a reasonable chance that using the product will cause serious health problems or death.
Class II: Using the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
Class III: Using the product is not likely to cause health problems (for example a labeling or packaging issue).
Next steps
- Find a pharmacy near youAsk which company made your medicine and whether it is recalled
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Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026