Heparin Sodium

Product NDC
0781-3327
11-digit product format
007813327
Labeler code
0781
Product ID
0781-3327_acd26ba3-bd84-48db-9824-07984dfb11df
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Heparin Sodium
Dosage form
INJECTION
Route
INTRAVENOUS; SUBCUTANEOUS
Labeler
Sandoz Inc
Application
ANDA091682
Marketing category
ANDA
Marketing start
2011-06-08
Marketing end
2020-04-30
Substance
HEPARIN SODIUM
Active strength
5000 [USP'U]/mL
Pharmacologic classes
Anti-coagulant [EPC],Heparin [CS],Unfractionated Heparin [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0781-3327-71ML - Milliliter0781-33276e24f08a-4886-4c74-b273-2176c824c52712017-03-06
0781-3327-95ML - Milliliter0781-33273a1f5239-2e0d-44ce-8e09-5fd9e4a5ccbe12017-03-06