0615-7722 : Escitalopram 20 mg Oral Tablet, Film Coated

NDC:	0615-7722
Labeler:	Ncs Healthcare of Ky, Inc Dba Vangard Labs
Product Type:	Human Prescription Drug
Drug Name:	Escitalopram
Dosage Form:	Oral Tablet, Film Coated
Application #:	ANDA076765
Rev. Date:	Mar 14, 2012

Appearance:

Markings:	5852;20
Shapes:	Round
Colors:	White
Size (mm):	10
Segments: ^*	2
^* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces.

5852 20: (0093-5852) Escitalopram 20 mg Oral Tablet, Film Coated by Ncs Healthcare of Ky, Inc Dba Vangard Labs

The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

0615-7722-05: 15 TABLET, FILM COATED IN 1 BLISTER PACK (0615‑7722‑05)
0615-7722-39: 30 TABLET, FILM COATED IN 1 BLISTER PACK (0615‑7722‑39)

Active Ingredients:

Escitalopram Oxalate

Dosage Strength:

20 mg

Inactive Ingredients:

Starch, Corn
Croscarmellose Sodium
Hypromellose 2910 (15 Mpa.s)
Magnesium Stearate
Mannitol
Cellulose, Microcrystalline
Polyethylene Glycol 6000
Titanium Dioxide

Pharmaceutical Classes:

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

NDC QR Code

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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.