Orange Book product · Generic (ANDA)
MANNITOL 25%
MANNITOL
At a glance
May 06, 1987
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 06, 1987
39 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
MANNITOL
Strength
12.5GM/50ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
ANDA 089240
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of MANNITOL
- 2020BRONCHITOLBrand (NDA)
NDA 202049 · PHARMAXIS EUROPE
- 2010ARIDOL KITBrand (NDA)
NDA 022368 · PHARMAXIS EUROPE
- 1993MANNITOL 10% IN PLASTIC CONTAINERBrand (NDA)
NDA 020006 · B BRAUN
- 1987MANNITOL 10% IN PLASTIC CONTAINERBrand (NDA)
NDA 019603 · OTSUKA ICU MEDCL
- —MANNITOL 10%Brand (NDA)
NDA 016080 · B BRAUN
- —MANNITOL 10%Brand (NDA)
NDA 016269 · HOSPIRA
- —MANNITOL 10%Brand (NDA)
NDA 016472 · MILES
- —MANNITOL 20%Brand (NDA)
NDA 014738 · B BRAUN
- —MANNITOL 25%Brand (NDA)
NDA 005620 · MERCK
- —OSMITROL 10% IN WATERBrand (NDA)
NDA 013684 · BAXTER HLTHCARE
- —RESECTISOLBrand (NDA)
NDA 016704 · B BRAUN
- —RESECTISOL IN PLASTIC CONTAINERBrand (NDA)
NDA 016772 · B BRAUN
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.
