ROPINIROLE HYDROCHLORIDE

Product NDC
64679-172
11-digit product format
646790172
Labeler code
64679
Product ID
64679-172_e5aa4d3e-9925-4d24-93ed-69a16f88601c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ropinirole hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Wockhardt USA LLC.
Application
ANDA079050
Marketing category
ANDA
Marketing start
2008-05-29
Marketing end
0000-00-00
Substance
ROPINIROLE HYDROCHLORIDE
Active strength
2 mg/1
Pharmacologic classes
Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
64679-172-02EA - Each64679-17203a9e104-7d8f-41e6-9627-089a1abe97d812012-07-24
64679-172-03EA - Each64679-1727f81d615-0205-4f40-b6e2-97ebccc1c40512012-07-24