NDC 69844-035

ESCITALOPRAM

Escitalopram Oxalate

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

Product ID69844-035_b17f059d-46ae-4160-9c55-7251ad243e30
NDC69844-035
Product TypeHuman Prescription Drug
Proprietary NameESCITALOPRAM
Generic NameEscitalopram Oxalate
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2019-11-14
Marketing CategoryANDA / ANDA
Application NumberANDA078777
Labeler NameGraviti Pharmaceuticals Private Limited
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 69844-035-01

30 TABLET, FILM COATED in 1 BOTTLE (69844-035-01)
Marketing Start Date2019-11-14
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69844-035-02 [69844003502]

ESCITALOPRAM TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078777
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-11-14

NDC 69844-035-01 [69844003501]

ESCITALOPRAM TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078777
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-11-14

NDC 69844-035-03 [69844003503]

ESCITALOPRAM TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078777
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-11-14

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 Oxalate"

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
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
70771-1146escitalopramescitalopram
70771-1147escitalopramescitalopram
70934-112EscitalopramEscitalopram
71205-168EscitalopramEscitalopram
71205-193EscitalopramEscitalopram
71335-0658EscitalopramEscitalopram
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.