Amitriptyline Hydrochloride

Product NDC
35356-742
11-digit product format
353560742
Labeler code
35356
Product ID
35356-742_54da0e4c-8478-498b-b100-fc09b2719c26
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amitriptyline Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Application
ANDA085968
Marketing category
ANDA
Marketing start
1977-11-29
Marketing end
0000-00-00
Substance
AMITRIPTYLINE HYDROCHLORIDE
Active strength
50 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
35356-742-30EA - Each35356-74247e9e7a2-1fa3-4178-a852-66f036eca80612013-02-13
35356-742-60EA - Each35356-742c0f8920b-86de-4792-a170-9d8366d4885712013-02-13
35356-742-90EA - Each35356-742b277da2e-0cbe-47d8-8678-a469890447a612013-02-13