0615-8366 : Escitalopram 20 mg Oral Tablet, Film Coated

NDC:	0615-8366
Labeler:	Ncs Healthcare of Ky, Inc Dba Vangard Labs
Product Type:	Human Prescription Drug
Drug Name:	Escitalopram
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA202389
Rev. Date:	Mar 21, 2013

NDC Package Codes:

0615-8366-05: 15 TABLET, FILM COATED IN 1 BLISTER PACK (0615‑8366‑05)
0615-8366-39: 30 TABLET, FILM COATED IN 1 BLISTER PACK (0615‑8366‑39)

Active Ingredients:

Escitalopram Oxalate

Dosage Strength:

20 mg

Pharmaceutical Classes:

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

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.