FDA.reportPublic FDA data

VENLAFAXINE HYDROCHLORIDE

Product NDC
31722-125
11-digit product format
317220125
Labeler code
31722
Product ID
31722-125_495259b8-9f81-4b6e-aa51-d199aa0edfb8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
venlafaxine
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Camber Pharmaceuticals, Inc.
Application
ANDA214419
Marketing category
ANDA
Marketing start
2020-10-23
Substance
VENLAFAXINE HYDROCHLORIDE
Active strength
150 mg/1
Pharmacologic classes
Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
VENLAFAXINE HYDROCHLORIDE
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
VENLAFAXINE HYDROCHLORIDE150 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii7D7RX5A8MO
Rxcui808744, 808748, 808751, 808753

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
17db3736-056c-48b9-b0f4-00fccabb14e6Product name520251118
7be8b949-f2c0-bdd8-e89d-8af92c1b2eadProduct name920250224
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
b1435b59-059c-404b-a587-53656bf80e17Product name120230314
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
6005cd75-f7b1-d6be-3cb5-4bd30d5c4617Product name320190314
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
d723478e-ad4a-ec23-6bd7-cfe33e1e3840Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
31722-125-30VENLAFAXINE HYDROCHLORIDE30 in 1 BOTTLETABLET, EXTENDED RELEASE302
31722-125-90VENLAFAXINE HYDROCHLORIDE90 in 1 BOTTLETABLET, EXTENDED RELEASE902

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
31722-125VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE) TABLET, EXTENDED RELEASE [CAMBER PHARMACEUTICALS, INC.]2Current NDC, Legacy NDC, 2 package rows20211120_8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd3.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
808744venlafaxine HCl 150 MG 24HR Extended Release Oral TabletPSN8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd32
808748venlafaxine HCl 225 MG 24HR Extended Release Oral TabletPSN8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd32
808751venlafaxine HCl 37.5 MG 24HR Extended Release Oral TabletPSN8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd32
808753venlafaxine HCl 75 MG 24HR Extended Release Oral TabletPSN8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd32
80874424 HR venlafaxine 150 MG Extended Release Oral TabletSCD8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd32
80874824 HR venlafaxine 225 MG Extended Release Oral TabletSCD8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd32
80875124 HR venlafaxine 37.5 MG Extended Release Oral TabletSCD8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd32
80875324 HR venlafaxine 75 MG Extended Release Oral TabletSCD8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd32
808744venlafaxine 150 MG (as venlafaxine hydrochloride) 24 HR Extended Release Oral TabletSY8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd32
808744venlafaxine 150 MG 24 HR Extended Release Oral TabletSY8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd32
808748venlafaxine 225 MG (as venlafaxine hydrochloride) 24 HR Extended Release Oral TabletSY8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd32
808748venlafaxine 225 MG 24 HR Extended Release Oral TabletSY8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd32
808751venlafaxine 37.5 MG (as venlafaxine hydrochloride) 24 HR Extended Release Oral TabletSY8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd32
808751venlafaxine 37.5 MG 24 HR Extended Release Oral TabletSY8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd32
808753venlafaxine 75 MG (as venlafaxine hydrochloride) 24 HR Extended Release Oral TabletSY8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd32
808753venlafaxine 75 MG 24 HR Extended Release Oral TabletSY8c4ccc5c-f6a2-4ce3-8866-9e6b32b08fd32

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
31722-125-303172201253030 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-125-30) 2020-10-230000-00-00NoNoCurrent
31722-125-903172201259090 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-125-90) 2020-10-230000-00-00NoNoCurrent