venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler teva pharmaceuticals usa, inc.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 150 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-7386
Product ID 0093-7386_4c5ca171-2a1c-4687-adf9-6d272463de4a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076565
Listing Expiration 2027-12-31
Marketing Start 2010-07-01

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 00937386
Hyphenated Format 0093-7386

Supplemental Identifiers

RxCUI
313581 313583 313585
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 ANDA076565 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-7386-05)
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-7386-56)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-7386-98)
source: ndc

Packages (3)

0093-7386-05 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-7386-05) 0093-7386-56 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-7386-56) 0093-7386-98 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-7386-98)

Ingredients (1)

venlafaxine hydrochloride (150 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": "4c5ca171-2a1c-4687-adf9-6d272463de4a", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["9a30e1b5-272b-4109-ad6c-a3c9a895822f"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-7386-05)", "package_ndc": "0093-7386-05", "marketing_start_date": "20120301"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-7386-56)", "package_ndc": "0093-7386-56", "marketing_start_date": "20100701"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-7386-98)", "package_ndc": "0093-7386-98", "marketing_start_date": "20100701"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "0093-7386_4c5ca171-2a1c-4687-adf9-6d272463de4a", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "0093-7386", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA076565", "marketing_category": "ANDA", "marketing_start_date": "20100701", "listing_expiration_date": "20271231"}