NDC 68788-9714

Escitalopram

Escitalopram Oxalate

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 ID: 68788-9714_c807ed8c-073b-4f26-8a57-60a3d0a32838
• NDC: 68788-9714
• Product Type: Human Prescription Drug
• Proprietary Name: Escitalopram
• Generic Name: Escitalopram Oxalate
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2013-01-18
• Marketing Category: ANDA / ANDA
• Application Number: ANDA090432
• Labeler Name: Preferred Pharmaceuticals, Inc.
• Substance Name: ESCITALOPRAM OXALATE
• Active Ingredient Strength: 10 mg/1
• Pharm Classes: Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 68788-9714-9

90 TABLET, FILM COATED in 1 BOTTLE (68788-9714-9)

• Marketing Start Date: 2013-01-18
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68788-9714-3 [68788971403]

Escitalopram TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA090432
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2013-01-18
• Marketing End Date: 2019-09-06

NDC 68788-9714-9 [68788971409]

Escitalopram TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA090432
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2013-01-18
• Marketing End Date: 2019-09-06

NDC 68788-9714-6 [68788971406]

Escitalopram TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA090432
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2013-01-18
• Marketing End Date: 2019-09-06

NDC 68788-9714-1 [68788971401]

Escitalopram TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA090432
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2013-01-18
• Marketing End Date: 2019-09-06

NDC 68788-9714-8 [68788971408]

Escitalopram TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA090432
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2013-01-18
• Marketing End Date: 2019-09-06

Drug Details

Active Ingredients

Ingredient	Strength
ESCITALOPRAM OXALATE	10 mg/1

OpenFDA Data

• SPL SET ID: 77eb8a63-bcbb-489c-9420-93dd8cc1d833
• Manufacturer:
  • Preferred Pharmaceuticals, Inc.
• UNII:
  • 5U85DBW7LO
• RxNorm Concept Unique ID - RxCUI:
  • 349332

Pharmacological Class

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

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

NDC	Brand Name	Generic Name
0093-5850	Escitalopram	Escitalopram
0093-5851	Escitalopram	Escitalopram
0093-5852	Escitalopram	Escitalopram
0143-9807	Escitalopram	Escitalopram
0143-9808	Escitalopram	Escitalopram
0143-9809	Escitalopram	Escitalopram
0615-7720	Escitalopram	Escitalopram
0615-7721	Escitalopram	Escitalopram
0615-7722	Escitalopram	Escitalopram
0615-7953	Escitalopram	Escitslopram
0615-7954	Escitalopram	Escitslopram
0615-7955	Escitalopram	Escitslopram
68001-195	Escitalopram	Escitalopram
68001-196	Escitalopram	Escitalopram
68001-197	Escitalopram	Escitalopram
68071-2051	Escitalopram	Escitalopram
68071-3069	Escitalopram	Escitalopram
68071-2035	Escitalopram	Escitalopram
68071-4332	Escitalopram	Escitalopram
68071-4484	Escitalopram	Escitalopram
68084-617	Escitalopram	Escitalopram
68084-618	Escitalopram	Escitalopram
68180-135	Escitalopram	Escitalopram
68180-136	Escitalopram	Escitalopram
68180-137	Escitalopram	Escitalopram
68258-7128	Escitalopram	Escitalopram
68382-103	escitalopram	escitalopram
68382-104	escitalopram	escitalopram
68382-102	escitalopram	escitalopram
68788-6837	Escitalopram	Escitalopram
68788-6403	Escitalopram	Escitalopram
68788-6783	Escitalopram	Escitalopram
68788-9302	Escitalopram	Escitalopram
68788-9456	Escitalopram	Escitalopram
68788-9714	Escitalopram	Escitalopram
70518-0692	Escitalopram	Escitalopram
70518-1110	Escitalopram	Escitalopram
70518-0758	Escitalopram	Escitalopram
70518-1103	Escitalopram	Escitalopram
70518-1857	Escitalopram	Escitalopram
70518-1876	Escitalopram	Escitalopram
70518-1785	Escitalopram	Escitalopram
70518-1805	Escitalopram	Escitalopram
70771-1145	escitalopram	escitalopram
70771-1146	escitalopram	escitalopram
70771-1147	escitalopram	escitalopram
70934-112	Escitalopram	Escitalopram
71205-168	Escitalopram	Escitalopram
71205-193	Escitalopram	Escitalopram
71335-0658	Escitalopram	Escitalopram