Paliperidone

Product NDC
70518-2197
11-digit product format
705182197
Labeler code
70518
Product ID
70518-2197_8d501073-251c-5139-e053-2995a90a330b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
paliperidone
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
NDA021999
Marketing category
NDA
Marketing start
2019-07-09
Marketing end
0000-00-00
Substance
PALIPERIDONE
Active strength
3 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record