Venlafaxine Hydrochloride

Product NDC: 68151-3659
11-digit product format: 681513659
Labeler code: 68151
Product ID: 68151-3659_badb18dd-50c6-4b08-8d72-c43a29f2fee4
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: VENLAFAXINE HYDROCHLORIDE
Dosage form: CAPSULE, EXTENDED RELEASE
Route: ORAL
Labeler: Carilion Materials Management
Application: NDA020699
Marketing category: NDA AUTHORIZED GENERIC
Marketing start: 2011-06-02
Marketing end: 0000-00-00
Substance: VENLAFAXINE HYDROCHLORIDE
Active strength: 38 mg/1
Pharmacologic classes: Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC exclude flag: E
Listing certified through: 2018-12-31
Current FDA listing: Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
17db3736-056c-48b9-b0f4-00fccabb14e6	Product name	5	20251118
7be8b949-f2c0-bdd8-e89d-8af92c1b2ead	Product name	9	20250224
b1435b59-059c-404b-a587-53656bf80e17	Product name	1	20230314
6005cd75-f7b1-d6be-3cb5-4bd30d5c4617	Product name	3	20190314

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68151-3659-7	2020-01-31	C162847	48780-1	9d75b9d0-31f3-f424-e053-dadaa90a57ce	These highlights do not include all the information needed to use VENLAFAXINE HYDROCHLORIDE EXTENDED-RELEASE safely and effectively. See full prescribing information for VENLAFAXINE HYDROCHLORIDE EXTENDED-RELEASE. Venlafaxine hydrochloride Extended-Release Capsules Initial U.S. Approval: 1997

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68151-3659-7	Venlafaxine Hydrochloride	1 in 1 CUP	CAPSULE, EXTENDED RELEASE	1		2

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68151-3659	VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [CARILION MATERIALS MANAGEMENT]	2	Legacy NDC, 1 package rows	20160213_505881c2-d0fe-4123-937e-41cc7a3f7243.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
7D7RX5A8MO	VENLAFAXINE HYDROCHLORIDE	99300-78-4	VENLAFAXINE HYDROCHLORIDE

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
313583	venlafaxine HCl 37.5 MG 24HR Extended Release Oral Capsule	PSN	505881c2-d0fe-4123-937e-41cc7a3f7243	2
313583	24 HR venlafaxine 37.5 MG Extended Release Oral Capsule	SCD	505881c2-d0fe-4123-937e-41cc7a3f7243	2
313583	venlafaxine (as venlafaxine HCl) 37.5 MG 24 HR Extended Release Oral Capsule	SY	505881c2-d0fe-4123-937e-41cc7a3f7243	2

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Status
68151-3659-7	68151365907	1 in 1 CUP	Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Venlafaxine Hydrochloride	Carilion Materials Management	2015-10-30	HUMAN PRESCRIPTION DRUG LABEL	2