NDC 68382-104

escitalopram

Escitalopram

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

• Product ID: 68382-104_1aea2c2e-60fe-4278-8963-58bce4e3fb96
• NDC: 68382-104
• Product Type: Human Prescription Drug
• Proprietary Name: escitalopram
• Generic Name: Escitalopram
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2017-12-07
• Marketing Category: ANDA / ANDA
• Application Number: ANDA077734
• Labeler Name: Zydus Pharmaceuticals (USA) Inc.
• Substance Name: ESCITALOPRAM OXALATE
• Active Ingredient Strength: 20 mg/1
• Pharm Classes: Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 68382-104-01

100 TABLET, FILM COATED in 1 BOTTLE (68382-104-01)

• Marketing Start Date: 2017-12-07
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68382-104-05 [68382010405]

escitalopram TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA077734
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-12-07

NDC 68382-104-06 [68382010406]

escitalopram TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA077734
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-12-07

NDC 68382-104-16 [68382010416]

escitalopram TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA077734
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-12-07

NDC 68382-104-01 [68382010401]

escitalopram TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA077734
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-12-07

NDC 68382-104-10 [68382010410]

escitalopram TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA077734
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-12-07

Drug Details

Active Ingredients

Ingredient	Strength
ESCITALOPRAM OXALATE	20 mg/1

OpenFDA Data

• SPL SET ID: 8f1db566-4401-4699-912e-a49f8b6a2de9
• Manufacturer:
  • Zydus Pharmaceuticals (USA) Inc.
• UNII:
  • 5U85DBW7LO
• RxNorm Concept Unique ID - RxCUI:
  • 351250
  • 349332
  • 351249

Pharmacological Class

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

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

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
0615-8348	Escitalopram	Escitalopram
0615-8349	Escitalopram	Escitalopram
0615-8350	Escitalopram	Escitalopram
0615-8365	Escitalopram	Escitalopram
0615-8366	Escitalopram	Escitalopram
16729-168	Escitalopram	Escitalopram
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