NDC 49884-948

Sapropterin Dihydrochloride 100 mg powder, for solution

On the label: ENDO USA, Inc..

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 ENDO USA, Inc. names for other drugs.

Product details

Generic drug
Sapropterin: every company that makes it
Form
powder, for solution, oral
Strength
100 mg
Approval
ANDA ANDA207207
On the market since
Oct 1, 2020
Package NDCs
49884-948-52 49884-948-72
Official label
DailyMed (National Library of Medicine), updated Jul 9, 2020

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