Heparin Sodium and Sodium Chloride

Product NDC
0338-9552
11-digit product format
003389552
Labeler code
0338
Product ID
0338-9552_4c7da5eb-fae8-4b18-9a17-6e4a3a193c8f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
heparin sodium
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Labeler
Baxter Healthcare Corporation
Marketing category
UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Marketing start
2017-10-25
Marketing end
0000-00-00
Substance
HEPARIN SODIUM
Active strength
2000 [iU]/1000mL
Pharmacologic classes
Anti-coagulant [EPC],Heparin [CS],Unfractionated Heparin [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0338-9552-10ML - Milliliter0338-9552853bf164-909e-4858-9c6d-3bb0f9dad09712018-02-20