Amitriptyline Hydrochloride

Product NDC
35356-712
11-digit product format
353560712
Labeler code
35356
Product ID
35356-712_50b19b03-ca40-42f7-a848-2f4483d06f3b
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
ANDA040218
Marketing category
ANDA
Marketing start
1997-09-11
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
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
35356-712-00EA - Each35356-7126316c619-74ca-4ae7-96aa-84b89dc6197a12012-07-24
35356-712-30EA - Each35356-712507083d6-145c-4fbd-a9f1-8eab2626e58c12015-10-02
35356-712-60EA - Each35356-7129fa58e1c-e033-4be3-b1a1-d20b04ed144512016-04-04
35356-712-90EA - Each35356-7125e2935cb-bb11-4736-91dd-08a01558c8ef12016-04-04