NDC 70771-1147

escitalopram

Escitalopram

escitalopram is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Cadila Healthcare Limited. The primary component is Escitalopram Oxalate.

Product ID70771-1147_456dcee0-a3e2-4cbc-9a33-91463a0d0430
NDC70771-1147
Product TypeHuman Prescription Drug
Proprietary Nameescitalopram
Generic NameEscitalopram
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2017-12-07
Marketing CategoryANDA / ANDA
Application NumberANDA077734
Labeler NameCadila Healthcare Limited
Substance NameESCITALOPRAM OXALATE
Active Ingredient Strength20 mg/1
Pharm ClassesSerotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 70771-1147-0

1000 TABLET, FILM COATED in 1 BOTTLE (70771-1147-0)
Marketing Start Date2017-12-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70771-1147-0 [70771114700]

escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077734
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-12-07

NDC 70771-1147-9 [70771114709]

escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077734
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-12-07

NDC 70771-1147-1 [70771114701]

escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077734
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-12-07

NDC 70771-1147-5 [70771114705]

escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077734
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-12-07

NDC 70771-1147-3 [70771114703]

escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077734
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-12-07

Drug Details

Active Ingredients

IngredientStrength
ESCITALOPRAM OXALATE20 mg/1

OpenFDA Data

SPL SET ID:76d0e2a8-2ed2-4596-9179-8c360f4a0978
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 351250
  • 349332
  • 351249

    • Pharmacological Class

    • Serotonin Reuptake Inhibitor [EPC]
    • Serotonin Uptake Inhibitors [MoA]

    NDC Crossover Matching brand name "escitalopram" or generic name "Escitalopram"

    NDCBrand NameGeneric Name
    0093-5850EscitalopramEscitalopram
    0093-5851EscitalopramEscitalopram
    0093-5852EscitalopramEscitalopram
    0143-9807EscitalopramEscitalopram
    0143-9808EscitalopramEscitalopram
    0143-9809EscitalopramEscitalopram
    0615-7720EscitalopramEscitalopram
    0615-7721EscitalopramEscitalopram
    0615-7722EscitalopramEscitalopram
    0615-7953EscitalopramEscitslopram
    0615-7954EscitalopramEscitslopram
    0615-7955EscitalopramEscitslopram
    0615-8348EscitalopramEscitalopram
    0615-8349EscitalopramEscitalopram
    0615-8350EscitalopramEscitalopram
    0615-8365EscitalopramEscitalopram
    0615-8366EscitalopramEscitalopram
    16729-168EscitalopramEscitalopram
    68001-195EscitalopramEscitalopram
    68001-196EscitalopramEscitalopram
    68001-197EscitalopramEscitalopram
    68071-2051EscitalopramEscitalopram
    68071-3069EscitalopramEscitalopram
    68071-2035EscitalopramEscitalopram
    68071-4332EscitalopramEscitalopram
    68071-4484EscitalopramEscitalopram
    68084-617EscitalopramEscitalopram
    68084-618EscitalopramEscitalopram
    68180-135EscitalopramEscitalopram
    68180-136EscitalopramEscitalopram
    68180-137EscitalopramEscitalopram
    68258-7128EscitalopramEscitalopram
    68382-103escitalopramescitalopram
    68382-104escitalopramescitalopram
    68382-102escitalopramescitalopram
    68788-6837EscitalopramEscitalopram
    68788-6403EscitalopramEscitalopram
    68788-6783EscitalopramEscitalopram
    68788-9302EscitalopramEscitalopram
    68788-9456EscitalopramEscitalopram
    68788-9714EscitalopramEscitalopram
    70518-0692EscitalopramEscitalopram
    70518-1110EscitalopramEscitalopram
    70518-0758EscitalopramEscitalopram
    70518-1103EscitalopramEscitalopram
    70518-1857EscitalopramEscitalopram
    70518-1876EscitalopramEscitalopram
    70518-1785EscitalopramEscitalopram
    70518-1805EscitalopramEscitalopram
    70771-1145escitalopramescitalopram
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.