ROPINIROLE HYDROCHLORIDE

Product NDC
64679-177
11-digit product format
646790177
Labeler code
64679
Product ID
64679-177_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
5 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
64679-177-02EA - Each64679-177cf16ed7a-9d5b-4542-9cac-9da9205a3dc712012-07-24