Nortriptyline Hydrochloride

Product NDC
71335-2459
11-digit product format
713352459
Labeler code
71335
Product ID
71335-2459_6b6c7607-6adb-4c42-a284-ba7684f8640d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nortriptyline Hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA073556
Marketing category
ANDA
Marketing start
2023-11-17
Substance
NORTRIPTYLINE HYDROCHLORIDE
Active strength
75 mg/1
Pharmacologic classes
Tricyclic Antidepressant [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
00FN6IH15DNORTRIPTYLINE HYDROCHLORIDE894-71-3NORTRIPTYLINE HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-2459-17133524590130 CAPSULE in 1 BOTTLE, PLASTIC (71335-2459-1) 30 capsule2024-08-22NoNoHistorical
71335-2459-27133524590260 CAPSULE in 1 BOTTLE, PLASTIC (71335-2459-2) 60 capsule2024-08-22NoNoHistorical
71335-2459-37133524590390 CAPSULE in 1 BOTTLE, PLASTIC (71335-2459-3) 90 capsule2024-08-22NoNoHistorical
71335-2459-47133524590428 CAPSULE in 1 BOTTLE, PLASTIC (71335-2459-4) 28 capsule2024-08-22NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Nortriptyline Hydrochloride Capsules, USPBryant Ranch Prepack2024-08-22HUMAN PRESCRIPTION DRUG LABEL1