tinzaparin Injectable Solution

Brand(s)
Innohep
Category(s)
prescription
SPL Type(s)
Human Prescription
Oldest Current Product
2010-07-01
License(s)
NDA
RxNORM
INJECTABLE SOLUTION\TINZAPARIN
FDAOB
INJECTION\INJECTION\TINZAPARIN SODIUM\rdfq
SPL Active
SUBCUTANEOUS\INJECTION, SOLUTION\TINZAPARIN SODIUM
SPL Moiety
SUBCUTANEOUS\INJECTION, SOLUTION\TINZAPARIN

product(s) by strength(s)

invalid application product(s)

#idbrandcategorylabelerfirst marketedactive ingredient(s)routedose formapplicationspl
1502220342InnohepNDALeo Pharma Inc.2010-07-01TINZAPARIN SODIUMSUBCUTANEOUSINJECTION, SOLUTIONNDA0204841513b960-d9d1-11de-8a1e-0002a5d5c51b

application(s)

#idtitledeprecatedapplicantapprovedapproved drug
1NDA020484INNOHEPTrueLEO PHARMA AS2000-07-14NDA020484_001

application drug(s)

#idcategory/deprecatedingredient strength(s)dose formrldapprovedapplication
1NDA020484_001discontinuedTINZAPARIN SODIUM (20,000 IU/ML)INJECTIONFalse2000-07-14INNOHEP

spl(s)

#idtitlecategorytypelabelerlabeler actlast updateversionproduct(s)
11513b960-d9d1-11de-8a1e-0002a5d5c51b (view SPL)INNOHEPRxonly (tinzaparin sodium injection)prescriptionHuman PrescriptionLeo Pharma Inc.ANALYSIS, API MANUFACTURE, LABEL, MANUFACTURE, PACK2010-10-055502220342

Data from: FDAOB, FDAPB, LOINC, MTHSPL, NDFRT, NCIT, RxNORM, UNII