Amitriptyline Hydrochloride

Product NDC
51079-133
11-digit product format
510790133
Labeler code
51079
Product ID
51079-133_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
1994-10-26
Marketing end
2021-01-31
Substance
AMITRIPTYLINE HYDROCHLORIDE
Active strength
50 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
51079-133-01EA - Each51079-13304c34a2c-433e-4f40-b467-9787042b37d912012-07-24
51079-133-20EA - Each51079-1338cd743bf-9f8f-4084-8d75-a9acc7f89b0f12012-07-24
51079-133-63EA - Each51079-1330450a901-6658-472c-9d87-87fe697605e812012-07-24