metaproterenol Oral Tablet

Category(s)
prescription
SPL Type(s)
Human Prescription
Master SPL
Par Pharmaceutical Companies, Inc. (2013-07-24)
Oldest Current Product
1988-06-28
License(s)
ANDA
RxNORM
ORAL TABLET\METAPROTERENOL
FDAOB
ORAL\TABLET\METAPROTERENOL SULFATE
SPL Active
ORAL\TABLET\METAPROTERENOL SULFATE
SPL Moiety
ORAL\TABLET\METAPROTERENOL

product(s) by strength(s)

metaproterenol sulfate 10 mg oral tablet

generic product(s)(s)

#idcategorylabelerfirst marketedactive ingredient(s)routedose formapplicationspl
1498840258ANDAPar Pharmaceutical Companies, Inc.1988-06-28METAPROTERENOL SULFATEORALTABLETANDA072024cf566e38-f6ff-4b86-9537-8684943b36eb

metaproterenol sulfate 20 mg oral tablet

generic product(s)(s)

#idcategorylabelerfirst marketedactive ingredient(s)routedose formapplicationspl
1498840259ANDAPar Pharmaceutical Companies, Inc.1988-06-28METAPROTERENOL SULFATEORALTABLETANDA072025cf566e38-f6ff-4b86-9537-8684943b36eb

application(s)

#idtitledeprecatedapplicantapprovedapproved drug
1ANDA071013METAPROTERENOL SULFATETrueUSL PHARMA INC1988-01-25ANDA071013_001
2ANDA071014METAPROTERENOL SULFATETrueUSL PHARMA INC1988-01-25ANDA071014_001
3ANDA072024METAPROTERENOL SULFATEPAR PHARMACEUTICAL INC1988-06-28ANDA072024_001
4ANDA072025METAPROTERENOL SULFATEPAR PHARMACEUTICAL INC1988-06-28ANDA072025_001
5ANDA072054METAPROTERENOL SULFATETrueAMERICAN THERAPEUTICS INC1988-06-23ANDA072054_001
6ANDA072055METAPROTERENOL SULFATETrueAMERICAN THERAPEUTICS INC1988-06-23ANDA072055_001
7ANDA072519METAPROTERENOL SULFATETrueTEVA PHARMACEUTICALS USA INC1990-03-30ANDA072519_001
8ANDA072520METAPROTERENOL SULFATETrueTEVA PHARMACEUTICALS USA INC1990-03-30ANDA072520_001
9ANDA072795METAPROTERENOL SULFATETrueWATSON LABORATORIES INC1991-01-31ANDA072795_001
10ANDA073013METAPROTERENOL SULFATETrueWATSON LABORATORIES INC1991-01-31ANDA073013_001
11NDA015874ALUPENTTrueBOEHRINGER INGELHEIM PHARMACEUTICALS INCNDA015874_001, NDA015874_002

application drug(s)

#idcategory/deprecatedingredient strength(s)routedose formrldapprovedapplication
1ANDA071013_001discontinuedMETAPROTERENOL SULFATE (10MG)ORALTABLETFalse1988-01-25METAPROTERENOL SULFATE
2ANDA071014_001discontinuedMETAPROTERENOL SULFATE (20MG)ORALTABLETFalse1988-01-25METAPROTERENOL SULFATE
3ANDA072024_001RXMETAPROTERENOL SULFATE (10MG)ORALTABLETFalse1988-06-28METAPROTERENOL SULFATE
4ANDA072025_001RXMETAPROTERENOL SULFATE (20MG)ORALTABLETTrue1988-06-28METAPROTERENOL SULFATE
5ANDA072054_001discontinuedMETAPROTERENOL SULFATE (10MG)ORALTABLETFalse1988-06-23METAPROTERENOL SULFATE
6ANDA072055_001discontinuedMETAPROTERENOL SULFATE (20MG)ORALTABLETFalse1988-06-23METAPROTERENOL SULFATE
7ANDA072519_001discontinuedMETAPROTERENOL SULFATE (10MG)ORALTABLETFalse1990-03-30METAPROTERENOL SULFATE
8ANDA072520_001discontinuedMETAPROTERENOL SULFATE (20MG)ORALTABLETFalse1990-03-30METAPROTERENOL SULFATE
9ANDA072795_001discontinuedMETAPROTERENOL SULFATE (20MG)ORALTABLETFalse1991-01-31METAPROTERENOL SULFATE
10ANDA073013_001discontinuedMETAPROTERENOL SULFATE (10MG)ORALTABLETFalse1991-01-31METAPROTERENOL SULFATE
11NDA015874_001discontinuedMETAPROTERENOL SULFATE (20MG)ORALTABLETFalseALUPENT
12NDA015874_002discontinuedMETAPROTERENOL SULFATE (10MG)ORALTABLETFalseALUPENT

spl(s)

#idtitlecategorytypelabelerlast updateversionproduct(s)
1cf566e38-f6ff-4b86-9537-8684943b36eb (view SPL)prescriptionHuman PrescriptionPar Pharmaceutical Companies, Inc.2013-07-244498840258, 498840259

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