Orange Book product · Brand (NDA)
NESACAINE-MPF
CHLOROPROCAINE HYDROCHLORIDE
Brand (NDA)NDA 009435TE APRX FRESENIUS KABI USA
At a glance
May 02, 1996
Approved
Brand (NDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 02, 1996
30 yr 7 mo ago
Today
Pharmaceutical detail
Active ingredient
CHLOROPROCAINE HYDROCHLORIDE
Strength
2%
Dosage form
INJECTABLE
Route
INJECTION
TE code
AP
Application
NDA 009435
Product number
006
Marketing status
RX
Reference listed drug (RLD)
Yes
Reference standard (RS)
Yes
Active-ingredient family
View full familyThis is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
