Nortriptyline Hydrochloride

Product NDC
71335-1743
11-digit product format
713351743
Labeler code
71335
Product ID
71335-1743_12b4dd22-76dd-498c-abd6-fc2d3ecdf0b2
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
10 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
71335-1743-1EA - Each71335-1743a699987a-f2cf-4d23-a0d8-4bcd6014b90812023-12-05

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1743-17133517430130 CAPSULE in 1 BOTTLE (71335-1743-1) 30 capsule2020-12-150000-00-00NoNoCurrent
71335-1743-27133517430260 CAPSULE in 1 BOTTLE (71335-1743-2) 60 capsule2020-12-150000-00-00NoNoCurrent
71335-1743-37133517430390 CAPSULE in 1 BOTTLE (71335-1743-3) 90 capsule2020-12-150000-00-00NoNoCurrent
71335-1743-471335174304100 CAPSULE in 1 BOTTLE (71335-1743-4) 100 capsule2020-12-150000-00-00NoNoCurrent
71335-1743-571335174305120 CAPSULE in 1 BOTTLE (71335-1743-5) 120 capsule2020-12-150000-00-00NoNoCurrent
71335-1743-67133517430615 CAPSULE in 1 BOTTLE (71335-1743-6) 15 capsule2020-12-150000-00-00NoNoCurrent