Orange Book product · Brand (NDA)
PHYSIOSOL IN PLASTIC CONTAINER
MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE
At a glance
Jul 08, 1982
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jul 08, 1982
44 yr 7 mo ago
Today
Pharmaceutical detail
Active ingredient
MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE
Strength
30MG/100ML;37MG/100ML;222MG/100ML;526MG/100ML;502MG/100ML
Dosage form
SOLUTION
Route
IRRIGATION
TE code
Not listed
Application
NDA 017637
Product number
002
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.
- 1989ISOLYTE S IN PLASTIC CONTAINERBrand (NDA)
NDA 019711 · B BRAUN
- 1985SYNOVALYTE IN PLASTIC CONTAINERBrand (NDA)
NDA 019326 · BAXTER HLTHCARE
- 1984PHYSIOLYTE IN PLASTIC CONTAINERBrand (NDA)
NDA 019024 · B BRAUN
- —ISOLYTE S IN PLASTIC CONTAINERBrand (NDA)
NDA 018252 · B BRAUN
- —NORMOSOL-R IN PLASTIC CONTAINERBrand (NDA)
NDA 017586 · OTSUKA ICU MEDCL
- —PLASMA-LYTE 148 IN WATER IN PLASTIC CONTAINERBrand (NDA)
NDA 017378 · BAXTER HLTHCARE
- —PHYSIOSOL IN PLASTIC CONTAINERBrand (NDA)
NDA 018406 · HOSPIRA INC
- 2022MULTIPLE ELECTROLYTES INJECTION TYPE 1 USP PH 5.5Generic (ANDA)
ANDA 215370 · FRESENIUS KABI USA
- 2022MULTIPLE ELECTROLYTES INJECTION TYPE 1 USP PH 7.4Generic (ANDA)
ANDA 215371 · 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.
