NDC 71335-0893

Tamoxifen Citrate

Tamoxifen Citrate

Tamoxifen Citrate is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Tamoxifen Citrate.

Product ID71335-0893_6d6d8113-69f2-4015-ad4f-db2306d245e1
NDC71335-0893
Product TypeHuman Prescription Drug
Proprietary NameTamoxifen Citrate
Generic NameTamoxifen Citrate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2003-02-20
Marketing CategoryANDA / ANDA
Application NumberANDA074732
Labeler NameBryant Ranch Prepack
Substance NameTAMOXIFEN CITRATE
Active Ingredient Strength20 mg/1
Pharm ClassesEstrogen Agonist/Antagonist [EPC],Selective Estrogen Receptor Modulators [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 71335-0893-1

30 TABLET in 1 BOTTLE (71335-0893-1)
Marketing Start Date2018-07-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0893-1 [71335089301]

Tamoxifen Citrate TABLET
Marketing CategoryANDA
Application NumberANDA074732
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-07-06

NDC 71335-0893-6 [71335089306]

Tamoxifen Citrate TABLET
Marketing CategoryANDA
Application NumberANDA074732
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-07-06

NDC 71335-0893-5 [71335089305]

Tamoxifen Citrate TABLET
Marketing CategoryANDA
Application NumberANDA074732
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-07-06

NDC 71335-0893-4 [71335089304]

Tamoxifen Citrate TABLET
Marketing CategoryANDA
Application NumberANDA074732
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-07-06

NDC 71335-0893-3 [71335089303]

Tamoxifen Citrate TABLET
Marketing CategoryANDA
Application NumberANDA074732
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-07-06

NDC 71335-0893-2 [71335089302]

Tamoxifen Citrate TABLET
Marketing CategoryANDA
Application NumberANDA074732
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-07-06

Drug Details

Active Ingredients

IngredientStrength
TAMOXIFEN CITRATE20 mg/1

OpenFDA Data

SPL SET ID:b02f410e-ba92-4853-9b67-2afbde9866be
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 313195

    • Pharmacological Class

    • Estrogen Agonist/Antagonist [EPC]
    • Selective Estrogen Receptor Modulators [MoA]

    NDC Crossover Matching brand name "Tamoxifen Citrate" or generic name "Tamoxifen Citrate"

    NDCBrand NameGeneric Name
    0179-0224Tamoxifen CitrateTamoxifen Citrate
    0378-0144Tamoxifen CitrateTamoxifen Citrate
    0378-0274Tamoxifen CitrateTamoxifen Citrate
    0591-2472Tamoxifen CitrateTamoxifen Citrate
    0591-2473Tamoxifen CitrateTamoxifen Citrate
    50090-0485Tamoxifen CitrateTamoxifen Citrate
    50090-0942Tamoxifen CitrateTamoxifen Citrate
    51407-439Tamoxifen CitrateTamoxifen Citrate
    51407-440Tamoxifen CitrateTamoxifen Citrate
    51862-446Tamoxifen CitrateTamoxifen Citrate
    51862-447Tamoxifen CitrateTamoxifen Citrate
    51862-449Tamoxifen CitrateTamoxifen Citrate
    51862-450Tamoxifen CitrateTamoxifen Citrate
    51862-642Tamoxifen CitrateTamoxifen Citrate
    51862-643Tamoxifen CitrateTamoxifen Citrate
    59651-299Tamoxifen CitrateTamoxifen Citrate
    59651-300Tamoxifen CitrateTamoxifen Citrate
    60429-909Tamoxifen CitrateTamoxifen Citrate
    60429-910Tamoxifen CitrateTamoxifen Citrate
    68382-827Tamoxifen CitrateTamoxifen Citrate
    68382-826Tamoxifen CitrateTamoxifen Citrate
    70518-1881Tamoxifen CitrateTamoxifen Citrate
    70771-1184Tamoxifen CitrateTamoxifen Citrate
    70771-1185Tamoxifen CitrateTamoxifen Citrate
    71335-0237Tamoxifen CitrateTamoxifen Citrate
    71335-0893Tamoxifen CitrateTamoxifen Citrate
    71335-0662Tamoxifen CitrateTamoxifen Citrate
    63187-976Tamoxifen CitrateTamoxifen Citrate
    63739-269Tamoxifen CitrateTamoxifen Citrate
    65084-269Tamoxifen CitrateTamoxifen Citrate
    68071-5005Tamoxifen CitrateTamoxifen Citrate
    71335-1424Tamoxifen CitrateTamoxifen Citrate
    68071-5254Tamoxifen CitrateTamoxifen Citrate
    70518-2721Tamoxifen CitrateTamoxifen Citrate
    51862-682SOLTAMOXTAMOXIFEN CITRATE
    © 2025 FDA.report
    This site is not affiliated with or endorsed by the FDA.