venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 225 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 47335-794
Product ID 47335-794_dae15132-d26b-4ea9-b937-da9c282ada48
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091272
Listing Expiration 2026-12-31
Marketing Start 2019-02-15

Pharmacologic Class

Classes
norepinephrine uptake inhibitors [moa] serotonin uptake inhibitors [moa] serotonin and norepinephrine reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 47335794
Hyphenated Format 47335-794

Supplemental Identifiers

RxCUI
808744 808748 808751 808753
UPC
0347335794830
UNII
7D7RX5A8MO

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name venlafaxine hydrochloride (source: ndc)
Generic Name venlafaxine hydrochloride (source: ndc)
Application Number ANDA091272 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 225 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-08)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-13)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-81)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-83)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-88)
  • 5 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-794-99) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (6)

47335-794-08 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-08) 47335-794-13 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-13) 47335-794-81 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-81) 47335-794-83 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-83) 47335-794-88 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-88) 47335-794-99 5 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-794-99) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (1)

venlafaxine hydrochloride (225 mg/1)

Linked Drug Pages (1)

Venlafaxine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "dae15132-d26b-4ea9-b937-da9c282ada48", "openfda": {"upc": ["0347335794830"], "unii": ["7D7RX5A8MO"], "rxcui": ["808744", "808748", "808751", "808753"], "spl_set_id": ["dc989aa7-c4ab-4359-a971-523eb477ef9b"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-08)", "package_ndc": "47335-794-08", "marketing_start_date": "20190215"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-13)", "package_ndc": "47335-794-13", "marketing_start_date": "20190215"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-81)", "package_ndc": "47335-794-81", "marketing_start_date": "20190815"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-83)", "package_ndc": "47335-794-83", "marketing_start_date": "20190215"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-88)", "package_ndc": "47335-794-88", "marketing_start_date": "20190215"}, {"sample": false, "description": "5 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-794-99)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "47335-794-99", "marketing_start_date": "20190215"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "47335-794_dae15132-d26b-4ea9-b937-da9c282ada48", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "47335-794", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "225 mg/1"}], "application_number": "ANDA091272", "marketing_category": "ANDA", "marketing_start_date": "20190215", "listing_expiration_date": "20261231"}