Amitriptyline Hydrochloride

Product NDC
51079-107
11-digit product format
510790107
Labeler code
51079
Product ID
51079-107_b4dca9ec-6443-a7e7-e053-2a95a90ad720
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
amitriptyline hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Mylan Institutional Inc.
Application
ANDA086009
Marketing category
ANDA
Marketing start
1994-02-15
Marketing end
2020-11-30
Substance
AMITRIPTYLINE HYDROCHLORIDE
Active strength
25 mg/1
Pharmacologic classes
Tricyclic Antidepressant [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51079-107-01EA - Each51079-107cb2e73ce-3fb4-4718-bf81-711b2f13286a12012-07-24
51079-107-17EA - Each51079-107b60e369a-d135-480b-8bba-df210e3dcf4712012-07-24
51079-107-19EA - Each51079-107cdd6fc0b-25b6-45d5-a5fa-146a1034bfe012012-07-24
51079-107-20EA - Each51079-107bbdebd4b-a1e1-4696-a226-e42ce2f6869312012-07-24
51079-107-63EA - Each51079-107838b56d7-08d2-4360-96b0-79cdd7d90a5912012-07-24