Lexapro

Product NDC: 55289-828
11-digit product format: 552890828
Labeler code: 55289
Product ID: 55289-828_dac069a2-9857-62f2-e053-2a95a90a2ca7
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: ESCITALOPRAM OXALATE
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: PD-Rx Pharmaceuticals, Inc.
Application: NDA021323
Marketing category: NDA
Marketing start: 2002-08-14
Marketing end: 0000-00-00
Substance: ESCITALOPRAM OXALATE
Active strength: 20 mg/1
Pharmacologic classes: Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
55289-828-30	EA - Each	55289-828	97625547-691c-4c0d-af63-d6eeb0771a2e	1	2012-07-24

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5U85DBW7LO	ESCITALOPRAM OXALATE	219861-08-2	ESCITALOPRAM OXALATE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
55289-828-30	55289082830	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-828-30)	2012-01-18	0000-00-00	No	No	Current