Doxepin Hydrochloride

Product NDC: 35356-650
11-digit product format: 353560650
Labeler code: 35356
Product ID: 35356-650_95afc67c-b3a1-4f98-a7b9-f0d0132db5ff
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: doxepin hydrochloride
Dosage form: CAPSULE
Route: ORAL
Labeler: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Application: ANDA070791
Marketing category: ANDA
Marketing start: 2012-04-03
Marketing end: 0000-00-00
Substance: DOXEPIN HYDROCHLORIDE
Active strength: 10 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#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
35356-650-30	2021-10-19	C162847	48780-1	ba0f9c33-56a4-a910-e053-dadaa90a0b85	7d745d52-ed8b-43cb-a672-aba1e0938ae8
35356-650-30	2021-01-29	C162847	48780-1	ba0f9c33-56a4-a910-e053-dadaa90a0b85	7d745d52-ed8b-43cb-a672-aba1e0938ae8

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
35356-650-30	EA - Each	35356-650	d9f917c5-5ac5-43c8-8cfd-3e7a4004ba74	1	2012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
35356-650-30	35356065030	30 CAPSULE in 1 BOTTLE, PLASTIC (35356-650-30)	30 capsule	2012-04-03	0000-00-00	No	No	Current