Orange Book product · Brand (NDA)
POTASSIUM CHLORIDE 20MEQ IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
POTASSIUM CHLORIDE; SODIUM CHLORIDE
At a glance
Oct 17, 1988
Approved
Brand (NDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Oct 17, 1988
38 yr 3 mo ago
Today
Pharmaceutical detail
Active ingredient
POTASSIUM CHLORIDE; SODIUM CHLORIDE
Strength
149MG/100ML;900MG/100ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
AP
Application
NDA 019686
Product number
001
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.
- 2002POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.45%Brand (NDA)
NDA 017648 · BAXTER HLTHCARE
- 1989POTASSIUM CHLORIDE 0.037% IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINERBrand (NDA)
NDA 019708 · B BRAUN
- 1982SODIUM CHLORIDE 0.9% AND POTASSIUM CHLORIDE 0.075% IN PLASTIC CONTAINERBrand (NDA)
NDA 018722 · B BRAUN
- 2020POTASSIUM CHLORIDE 0.15% IN SODIUM CHLORIDE 0.45%Generic (ANDA)
ANDA 212347 · FRESENIUS KABI USA
- 2008POTASSIUM CHLORIDE 0.149% IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINERGeneric (ANDA)
ANDA 078446 · OTSUKA ICU MEDCL
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.
