NDC 71205-344

Escitalopram

Escitalopram

Escitalopram is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Proficient Rx Lp. The primary component is Escitalopram Oxalate.

Product ID71205-344_2fb28a40-037a-49a0-b418-6c6841885cf4
NDC71205-344
Product TypeHuman Prescription Drug
Proprietary NameEscitalopram
Generic NameEscitalopram
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2013-03-19
Marketing CategoryANDA / ANDA
Application NumberANDA202389
Labeler NameProficient Rx LP
Substance NameESCITALOPRAM OXALATE
Active Ingredient Strength10 mg/1
Pharm ClassesSerotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71205-344-30

30 TABLET, FILM COATED in 1 BOTTLE (71205-344-30)
Marketing Start Date2019-11-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71205-344-30 [71205034430]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA202389
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-11-01

NDC 71205-344-60 [71205034460]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA202389
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-11-01

NDC 71205-344-90 [71205034490]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA202389
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-11-01

Drug Details

Active Ingredients

IngredientStrength
ESCITALOPRAM OXALATE10 mg/1

Pharmacological Class

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