Heparin Sodium

Product NDC
0409-0012
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
HEPARIN SODIUM
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Labeler
Hospira, Inc.
Application
NDA018916
Marketing category
NDA
Substance
HEPARIN SODIUM
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
0409-0012-3030 POUCH in 1 CASE (0409-0012-30) / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0409-0012-02) 2023-02-27NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Heparin SodiumHospira, Inc.2026-05-12HUMAN PRESCRIPTION DRUG LABEL31