Nortriptyline Hydrochloride

Product NDC
35356-651
11-digit product format
353560651
Labeler code
35356
Product ID
35356-651_eb834045-6333-4d82-9b2a-1d221d1d89c0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nortriptyline Hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA073553
Marketing category
ANDA
Marketing start
1992-07-01
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
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
35356-651-30EA - Each35356-65133dbbb08-e3ab-44f3-a63d-9a2f63720fe612013-06-04
35356-651-60EA - Each35356-65175322720-7566-4a6c-8035-eb25b3f512db12013-06-04