Venlafaxine Hydrochloride

Product NDC
59762-0180
11-digit product format
597620180
Labeler code
59762
Product ID
59762-0180_efcd1626-4fc3-494a-bb29-05e2255d2c1c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
VENLAFAXINE HYDROCHLORIDE
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
Greenstone LLC
Application
NDA020699
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2011-06-02
Marketing end
2019-09-30
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
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
17db3736-056c-48b9-b0f4-00fccabb14e6Product name520251118
7be8b949-f2c0-bdd8-e89d-8af92c1b2eadProduct name920250224
b1435b59-059c-404b-a587-53656bf80e17Product name120230314
6005cd75-f7b1-d6be-3cb5-4bd30d5c4617Product name320190314

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59762-0180-1EA - Each59762-0180d2f76997-e4d1-4001-b7f3-90209c11c67d12012-07-24
59762-0180-2EA - Each59762-0180b0606978-5ce5-4838-9cf6-8b6e5d1979ed12012-07-24
59762-0180-3EA - Each59762-0180f6f67f1c-f89b-4138-84ad-e6b28032a1c912012-07-24
59762-0180-4EA - Each59762-0180c0260bef-43c4-47d3-bc4d-186663bd48da12012-07-24

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
313583venlafaxine HCl 37.5 MG 24HR Extended Release Oral CapsulePSN505881c2-d0fe-4123-937e-41cc7a3f72432
31358324 HR venlafaxine 37.5 MG Extended Release Oral CapsuleSCD505881c2-d0fe-4123-937e-41cc7a3f72432
313583venlafaxine (as venlafaxine HCl) 37.5 MG 24 HR Extended Release Oral CapsuleSY505881c2-d0fe-4123-937e-41cc7a3f72432