NDC 70518-2521

Escitalopram

Escitslopram

Escitalopram is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Remedyrepack Inc.. The primary component is Escitalopram Oxalate.

Product ID70518-2521_9b7116be-81f8-31cb-e053-2995a90aaf10
NDC70518-2521
Product TypeHuman Prescription Drug
Proprietary NameEscitalopram
Generic NameEscitslopram
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2020-01-03
Marketing CategoryANDA / ANDA
Application NumberANDA078169
Labeler NameREMEDYREPACK INC.
Substance NameESCITALOPRAM OXALATE
Active Ingredient Strength10 mg/1
Pharm ClassesSerotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 70518-2521-0

30 TABLET in 1 BLISTER PACK (70518-2521-0)
Marketing Start Date2020-01-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70518-2521-0 [70518252100]

Escitalopram TABLET
Marketing CategoryANDA
Application NumberANDA078169
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2020-01-03

Drug Details

Active Ingredients

IngredientStrength
ESCITALOPRAM OXALATE10 mg/1

Pharmacological Class

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

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

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.