Orange Book product · Brand (NDA)
POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% IN PLASTIC CONTAINER
DEXTROSE; POTASSIUM CHLORIDE
At a glance
Sep 29, 1989
Approved
Brand (NDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Sep 29, 1989
37 yr 3 mo ago
Today
Pharmaceutical detail
Active ingredient
DEXTROSE; POTASSIUM CHLORIDE
Strength
5GM/100ML;150MG/100ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
AP
Application
NDA 019699
Product number
004
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a brand (NDA) product. Other products sharing this active ingredient are listed below.
- 1982POTASSIUM CHLORIDE 0.075% IN DEXTROSE 5% IN PLASTIC CONTAINERBrand (NDA)
NDA 018744 · B BRAUN
- —DEXTROSE 5% AND POTASSIUM CHLORIDE 0.075% IN PLASTIC CONTAINERBrand (NDA)
NDA 017634 · BAXTER HLTHCARE
- —POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% IN PLASTIC CONTAINERBrand (NDA)
NDA 018371 · OTSUKA ICU MEDCL
- 2020DEXTROSE 5% AND POTASSIUM CHLORIDE 0.075%Generic (ANDA)
ANDA 212346 · FRESENIUS KABI USA
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.
