Orange Book product · Brand (NDA)
POTASSIUM CHLORIDE 10MEQ IN PLASTIC CONTAINER
POTASSIUM CHLORIDE
At a glance
Nov 30, 1992
Approved
Brand (NDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Nov 30, 1992
34 yr ago
Today
Pharmaceutical detail
Active ingredient
POTASSIUM CHLORIDE
Strength
14.9MG/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
AP
Application
NDA 020161
Product number
005
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.
- 2023POKONZABrand (NDA)
NDA 208019 · GENUS
- 1988MICRO-K LSBrand (NDA)
NDA 019561 · KV PHARM
- —MICRO-KBrand (NDA)
NDA 018238 · NESHER PHARMS
- 2025POTASSIUM CHLORIDEGeneric (ANDA)
ANDA 219009 · ANDA REPOSITORY
- 2023POTASSIUM CHLORIDEGeneric (ANDA)
ANDA 212816 · NOVITIUM PHARMA
- 2022POTASSIUM CHLORIDEGeneric (ANDA)
ANDA 214108 · RUBICON RESEARCH
- 2022POTASSIUM CHLORIDEGeneric (ANDA)
ANDA 213467 · GRANULES
- 2021POTASSIUM CHLORIDEGeneric (ANDA)
ANDA 211667 · STRIDES PHARMA
- 2021POTASSIUM CHLORIDEGeneric (ANDA)
ANDA 214686 · GRANULES
- 2019POTASSIUM CHLORIDEGeneric (ANDA)
ANDA 209026 · PRINSTON INC
- 2019POTASSIUM CHLORIDEGeneric (ANDA)
ANDA 210902 · AMNEAL
- 2019POTASSIUM CHLORIDEGeneric (ANDA)
ANDA 212183 · AJENAT PHARMS
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.
