Orange Book product · Brand (NDA)
SODIUM LACTATE 1/6 MOLAR IN PLASTIC CONTAINER
SODIUM LACTATE
At a glance
Apr 21, 1992
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Apr 21, 1992
34 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
SODIUM LACTATE
Strength
1.87GM/100ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
NDA 020004
Product number
001
Marketing status
DISCN
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.
- 1984SODIUM LACTATE IN PLASTIC CONTAINERBrand (NDA)
NDA 018947 · HOSPIRA
- —SODIUM LACTATE 0.167 MOLAR IN PLASTIC CONTAINERBrand (NDA)
NDA 018186 · B BRAUN
- —SODIUM LACTATE 0.167 MOLAR IN PLASTIC CONTAINERBrand (NDA)
NDA 016692 · BAXTER HLTHCARE
- —SODIUM LACTATE 0.167 MOLAR IN PLASTIC CONTAINERBrand (NDA)
NDA 018249 · HOSPIRA
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.
