Pramipexole Dihydrochloride

Product NDC
0781-5252
11-digit product format
007815252
Labeler code
0781
Product ID
0781-5252_57121d70-d083-4862-b4e5-c69e12067089
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pramipexole Dihydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Sandoz Inc
Application
ANDA090190
Marketing category
ANDA
Marketing start
2010-07-06
Marketing end
0000-00-00
Substance
PRAMIPEXOLE DIHYDROCHLORIDE
Active strength
2 mg/1
Pharmacologic classes
Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]
NDC exclude flag
E
Listing certified through
2018-12-31
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
0781-5252-92EA - Each0781-525212551359-e05c-4cf0-9f9b-6c02109db19512012-07-24