NDC 68788-7461

Escitalopram

Escitalopram

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

Product ID68788-7461_32768da2-112a-4f7a-966e-c282aa056356
NDC68788-7461
Product TypeHuman Prescription Drug
Proprietary NameEscitalopram
Generic NameEscitalopram
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2012-03-15
Marketing CategoryANDA / ANDA
Application NumberANDA078032
Labeler NamePreferred Pharmaceuticals, Inc.
Substance NameESCITALOPRAM OXALATE
Active Ingredient Strength20 mg/1
Pharm ClassesSerotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 68788-7461-1

100 TABLET, FILM COATED in 1 BOTTLE (68788-7461-1)
Marketing Start Date2019-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-7461-3 [68788746103]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078032
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-27

NDC 68788-7461-1 [68788746101]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078032
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-27

NDC 68788-7461-8 [68788746108]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078032
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-27

NDC 68788-7461-9 [68788746109]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078032
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-27

NDC 68788-7461-6 [68788746106]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078032
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-27

Drug Details

Active Ingredients

IngredientStrength
ESCITALOPRAM OXALATE20 mg/1

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

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