AMITRIPTYLINE HYDROCHLORIDE

Product NDC
50090-2840
11-digit product format
500902840
Labeler code
50090
Product ID
50090-2840_0e6d3575-3408-448c-a577-972d345c42df
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
AMITRIPTYLINE HYDROCHLORIDE
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA202446
Marketing category
ANDA
Marketing start
2014-12-05
Marketing end
0000-00-00
Substance
AMITRIPTYLINE HYDROCHLORIDE
Active strength
25 mg/1
Pharmacologic classes
Tricyclic Antidepressant [EPC]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-2840-0EA - Each50090-2840580b58c7-e54e-45a7-8d61-a1525946c74412020-03-10
50090-2840-1EA - Each50090-2840b7586ef2-b6da-4d4e-81f4-17e8b69dd93312019-04-11
50090-2840-4EA - Each50090-2840dca2eca0-c60d-4902-b686-14fa679316b212019-04-11
50090-2840-8EA - Each50090-2840fb7087a8-4a62-4c51-bea0-542ae637477c12020-03-10

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
50090-2840-05009028400030 TABLET, FILM COATED in 1 BOTTLE (50090-2840-0) 2018-08-100000-00-00NoNoCurrent
50090-2840-150090284001100 TABLET, FILM COATED in 1 BOTTLE (50090-2840-1) 2018-08-140000-00-00NoNoCurrent
50090-2840-45009028400460 TABLET, FILM COATED in 1 BOTTLE (50090-2840-4) 2017-02-030000-00-00NoNoCurrent
50090-2840-85009028400890 TABLET, FILM COATED in 1 BOTTLE (50090-2840-8) 2018-09-120000-00-00NoNoCurrent