Menopur 9 mg / 75 [iU] kit

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Ferring Pharmaceuticals Inc. names for other drugs.

Recalls

• Mar 2, 2021 · Class III · Ferring Pharmaceuticals Inc
  Failed pH specifications: Out of Specification pH results for 0.9% Sodium Chloride, USP
  Lots: Lots# a) P12585AC, Exp. Date 31-Mar-2020 P12677AA, Exp. Date 31-Mar-2020 P12678AA, Exp. Date 31-Jul-2020 P12679AA, Exp. Date 31-Jul-2020 P12680EA, Exp. Date 31-Jul-2020 P15461AA, Exp. Date 31-Jul-2020 P15462AA, Exp. Date 31-Aug-2020 P15463AA, Exp. Date 31-Aug-2020 …

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Chloride Ion and Follitropin and Luteinizing Hormone: every company that makes it

Form

kit

Strength

9 mg / 75 [iU]

Approval

BLA BLA021663

On the market since

Oct 29, 2004

Package NDCs

55566-1600-0 55566-7501-1 55566-7501-2 55566-7502-0

Official label

DailyMed (National Library of Medicine), updated May 31, 2018

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?