Nortriptyline Hydrochloride

Product NDC
71335-1726
11-digit product format
713351726
Labeler code
71335
Product ID
71335-1726_308ab3ae-000a-4f77-bebf-4288e67555a1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nortriptyline Hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA073556
Marketing category
ANDA
Marketing start
2019-12-12
Marketing end
0000-00-00
Substance
NORTRIPTYLINE HYDROCHLORIDE
Active strength
25 mg/1
Pharmacologic classes
Tricyclic Antidepressant [EPC]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71335-1726-2EA - Each71335-1726b5567661-0084-442c-8dab-ad07c874f7be12022-07-06
71335-1726-4EA - Each71335-1726993d9159-483a-493d-9177-f155ca93b7e312022-07-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1726-27133517260260 CAPSULE in 1 BOTTLE (71335-1726-2) 60 capsule2020-11-030000-00-00NoNoCurrent
71335-1726-47133517260430 CAPSULE in 1 BOTTLE (71335-1726-4) 30 capsule2020-11-030000-00-00NoNoCurrent
71335-1726-57133517260590 CAPSULE in 1 BOTTLE (71335-1726-5) 90 capsule2020-11-030000-00-00NoNoCurrent
71335-1726-67133517260650 CAPSULE in 1 BOTTLE (71335-1726-6) 50 capsule2020-11-030000-00-00NoNoCurrent
71335-1726-771335172607100 CAPSULE in 1 BOTTLE (71335-1726-7) 100 capsule2020-11-030000-00-00NoNoCurrent
71335-1726-871335172608120 CAPSULE in 1 BOTTLE (71335-1726-8) 120 capsule2020-11-030000-00-00NoNoCurrent
71335-1726-97133517260928 CAPSULE in 1 BOTTLE (71335-1726-9) 28 capsule2020-11-030000-00-00NoNoCurrent