Escitalopram

Product NDC: 42708-022
11-digit product format: 427080022
Labeler code: 42708
Product ID: 42708-022_bd5aae99-dac6-051c-e053-2a95a90a2eef
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Escitalopram
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: QPharma Inc
Application: ANDA076765
Marketing category: ANDA
Marketing start: 2012-03-14
Marketing end: 0000-00-00
Substance: ESCITALOPRAM OXALATE
Active strength: 10 mg/1
Pharmacologic classes: Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
42708-022-30	2021-03-12	C162847	48780-1	ba0f9c33-4704-a910-e053-dadaa90a0b85	4940236b-f689-4914-ac81-4e077d6010f0
42708-022-30	2021-01-29	C162847	48780-1	ba0f9c33-4704-a910-e053-dadaa90a0b85	4940236b-f689-4914-ac81-4e077d6010f0

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5U85DBW7LO	ESCITALOPRAM OXALATE	219861-08-2	ESCITALOPRAM OXALATE
4O4S742ANY	ESCITALOPRAM	128196-01-0	Escitalopram

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
42708-022-30	42708002230	30 TABLET, FILM COATED in 1 BOTTLE (42708-022-30)	2018-03-29	0000-00-00	Yes	No	Current