SERTRALINE HYDROCHLORIDE

Product NDC
55289-381
11-digit product format
552890381
Labeler code
55289
Product ID
55289-381_85c98dce-3b9b-0867-e053-2a91aa0addc6
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
sertraline hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
NDA019839
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
1992-02-11
Marketing end
0000-00-00
Substance
SERTRALINE HYDROCHLORIDE
Active strength
100 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55289-381-30EA - Each55289-3810bd0bd18-6f47-4b2d-ad7c-76bdf753cebc12012-07-24
55289-381-45EA - Each55289-3810df56b33-3993-43be-8386-12c02abdd8b512012-07-24
55289-381-60EA - Each55289-38166085096-bf0c-450f-bb51-2a72803baa9a12012-07-24
55289-381-90EA - Each55289-38191b957f4-2a3e-432f-9b27-85b00c6ed60812012-07-24