Allopurinol Injection

Brand(s)
Aloprim
Category(s)
prescription
SPL Type(s)
Human Prescription
Master SPL
Mylan Institutional Llc (2014-06-30)
Oldest Current Product
1996-05-01
License(s)
NDA
RxNORM
INJECTION\ALLOPURINOL
FDAOB
INJECTION\INJECTION\ALLOPURINOL SODIUM\rdfq
SPL Active
INTRAVENOUS\INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION\ALLOPURINOL
SPL Moiety
INTRAVENOUS\INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION\ALLOPURINOL

product(s) by strength(s)

allopurinol 500 mg injection

original product(s)(s)

#idbrandcategorylabelerfirst marketedactive ingredient(s)routedose formapplicationspl
1674570187AloprimNDAMylan Institutional Llc1996-05-01ALLOPURINOLINTRAVENOUSINJECTION, POWDER, LYOPHILIZED, FOR SOLUTIONNDA02029810cc918f-aa44-415b-932d-2404695ac449

application(s)

#idtitleapplicantapprovedapproved drug
1ANDA076870ALLOPURINOL SODIUMEUROHEALTH INTERNATIONAL SARL2004-08-26ANDA076870_001
2NDA020298ALOPRIMMYLAN INSTITUTIONAL LLC1996-05-17NDA020298_001

application drug(s)

#idcategory/deprecatedingredient strength(s)dose formrldTEapprovedapplication
1ANDA076870_001RXALLOPURINOL SODIUM (EQ 500MG BASE/VIAL)INJECTIONFalseAP2004-08-26ALLOPURINOL SODIUM
2NDA020298_001RXALLOPURINOL SODIUM (EQ 500MG BASE/VIAL)INJECTIONTrueAP1996-05-17ALOPRIM

spl(s)

#idtitlecategorytypelabelerlast updateversionproduct(s)
110cc918f-aa44-415b-932d-2404695ac449 (view SPL)ALOPRIM (allopurinol sodium) for InjectionprescriptionHuman PrescriptionMylan Institutional Llc2014-06-304674570187

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