NDC 71335-0322

escitalopram oxalate

Escitalopram Oxalate

escitalopram oxalate is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Escitalopram Oxalate.

Product ID71335-0322_72e39981-3959-4fa1-9a5e-54c00b7e96e5
NDC71335-0322
Product TypeHuman Prescription Drug
Proprietary Nameescitalopram oxalate
Generic NameEscitalopram Oxalate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2012-09-11
Marketing CategoryANDA /
Application NumberANDA090939
Labeler NameBryant Ranch Prepack
Substance NameESCITALOPRAM OXALATE
Active Ingredient Strength10 mg/1
Pharm ClassesSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 71335-0322-1

30 TABLET in 1 BOTTLE (71335-0322-1)
Marketing Start Date2022-05-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0322-4 [71335032204]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-09-11
Marketing End Date2018-08-31

NDC 71335-0322-5 [71335032205]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-09-11
Marketing End Date2018-08-31

NDC 71335-0322-2 [71335032202]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-09-11
Marketing End Date2018-08-31

NDC 71335-0322-6 [71335032206]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-09-11
Marketing End Date2018-08-31

NDC 71335-0322-1 [71335032201]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-09-11
Marketing End Date2018-08-31

NDC 71335-0322-7 [71335032207]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-09-11
Marketing End Date2018-08-31

NDC 71335-0322-3 [71335032203]

escitalopram oxalate TABLET
Marketing CategoryANDA
Application NumberANDA090939
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-09-11
Marketing End Date2018-08-31

Drug Details

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

NDCBrand NameGeneric Name
0121-0852Escitalopram OxalateEscitalopram Oxalate
0378-3855Escitalopram Oxalateescitalopram
0378-3856Escitalopram Oxalateescitalopram
0378-3857Escitalopram Oxalateescitalopram
0904-6426escitalopram oxalateescitalopram oxalate
0904-6427escitalopram oxalateescitalopram oxalate
10544-224escitalopram oxalateescitalopram oxalate
10544-225escitalopram oxalateescitalopram oxalate
10544-230escitalopram oxalateescitalopram oxalate
10544-968Escitalopram Oxalateescitalopram
10544-969Escitalopram Oxalateescitalopram
13668-135escitalopram oxalateescitalopram oxalate
13668-136escitalopram oxalateescitalopram oxalate
13668-137escitalopram oxalateescitalopram oxalate
68071-3283Escitalopram OxalateEscitalopram Oxalate
68071-3312escitalopram oxalateescitalopram oxalate
68071-3265escitalopram oxalateescitalopram oxalate
68071-4210escitalopram oxalateescitalopram oxalate
68645-519Escitalopram OxalateEscitalopram Oxalate
68645-520Escitalopram OxalateEscitalopram Oxalate
68788-6978escitalopram oxalateescitalopram oxalate
69097-848Escitalopram OxalateEscitalopram Oxalate
69097-849Escitalopram OxalateEscitalopram Oxalate
69097-847Escitalopram OxalateEscitalopram Oxalate
70518-0467escitalopram oxalateescitalopram oxalate
70518-0472escitalopram oxalateescitalopram oxalate
70518-0439escitalopram oxalateescitalopram oxalate
70518-1315escitalopram oxalateescitalopram oxalate
70518-0972Escitalopram OxalateEscitalopram Oxalate
70518-0791escitalopram oxalateescitalopram oxalate
70518-1291escitalopram oxalateescitalopram oxalate
70518-1697escitalopram oxalateescitalopram oxalate
70934-060escitalopram oxalateescitalopram oxalate
70934-089escitalopram oxalateescitalopram oxalate
70934-163escitalopram oxalateescitalopram oxalate
71335-0685escitalopram oxalateescitalopram oxalate
76282-251Escitalopram oxalateEscitalopram oxalate
76282-249Escitalopram oxalateEscitalopram oxalate
76282-250Escitalopram oxalateEscitalopram oxalate
31722-569Escitalopram OxalateEscitalopram Oxalate
33261-955escitalopram oxalateescitalopram oxalate
33342-036Escitalopram OxalateEscitalopram Oxalate
33342-038Escitalopram OxalateEscitalopram Oxalate
33342-037Escitalopram OxalateEscitalopram Oxalate
43063-761escitalopram oxalateescitalopram oxalate
50090-2752escitalopram oxalateescitalopram oxalate
51079-544Escitalopram OxalateEscitalopram Oxalate
51079-543Escitalopram OxalateEscitalopram Oxalate
55154-5386Escitalopram OxalateEscitalopram Oxalate
54838-551Escitalopram OxalateEscitalopram Oxalate

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