Orange Book product · Brand (NDA)
HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
HEPARIN SODIUM
At a glance
Jan 31, 1984
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 31, 1984
43 yr ago
Today
Pharmaceutical detail
Active ingredient
HEPARIN SODIUM
Strength
10,000 UNITS/100ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
NDA 018916
Product number
008
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.
- 2011HEPARIN SODIUMBrand (NDA)
NDA 201370 · PFIZER
- —HEPARIN LOCK FLUSHBrand (NDA)
NDA 005264 · HOSPIRA
- —HEPARIN LOCK FLUSHBrand (NDA)
NDA 017346 · PARKE DAVIS
- —HEPARIN SODIUMBrand (NDA)
NDA 017033 · ABRAXIS PHARM
- —HEPARIN SODIUMBrand (NDA)
NDA 017979 · ABRAXIS PHARM
- —HEPARIN SODIUMBrand (NDA)
NDA 000552 · ASPEN GLOBAL INC
- —HEPARIN SODIUMBrand (NDA)
NDA 017130 · CHAMBERLIN PARENTERL
- —HEPARIN SODIUMBrand (NDA)
NDA 017540 · DELL LABS
- —HEPARIN SODIUMBrand (NDA)
NDA 017064 · DR REDDYS
- —HEPARIN SODIUMBrand (NDA)
NDA 017486 · EPIC PHARMA LLC
- —HEPARIN SODIUMBrand (NDA)
NDA 017029 · FRESENIUS KABI USA
- —HEPARIN SODIUMBrand (NDA)
NDA 017651 · 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.
