Amitriptyline Hydrochloride

Product NDC
50090-0030
11-digit product format
500900030
Labeler code
50090
Product ID
50090-0030_65b0e128-fcf7-4de7-ba34-1cb9367e0d55
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amitriptyline Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA040218
Marketing category
ANDA
Marketing start
1997-09-11
Marketing end
0000-00-00
Substance
AMITRIPTYLINE H
Active strength
10 mg/1
Pharmacologic classes
Tricyclic Antid
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
50090-0030-0EA - Each50090-003061a43987-d56c-433b-ac62-be5edc11adeb12018-08-13
50090-0030-1EA - Each50090-00305357d27b-2eb0-4d67-95b0-a27910e5e34a12018-08-13
50090-0030-6EA - Each50090-0030ed450691-43b4-4f66-83aa-c448a7bdd60b12018-08-13