NDC 71034-002

Pramipexole Dihydrochloride Extended-Release 0.375 mg tablet, extended release

On the label: Xiamen LP Pharmaceutical Co., Ltd..

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 Xiamen LP Pharmaceutical Co., Ltd. names for other drugs.

Product details

Generic drug
Pramipexole: every company that makes it
Form
tablet, extended release, oral
Strength
0.375 mg
Approval
ANDA ANDA212797
On the market since
Jun 11, 2021
Package NDCs
71034-002-30
Official label
DailyMed (National Library of Medicine), updated Jun 16, 2021

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