venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler a-s medication solutions
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 75 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-2180
Product ID 50090-2180_4fb50561-0316-46fa-927e-4b33441de698
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200834
Listing Expiration 2026-12-31
Marketing Start 2011-06-01

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 500902180
Hyphenated Format 50090-2180

Supplemental Identifiers

RxCUI
313581 313583 313585
UNII
7D7RX5A8MO

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 ANDA200834 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-2180-0)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-2180-1)
source: ndc

Packages (2)

50090-2180-0 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-2180-0) 50090-2180-1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-2180-1)

Ingredients (1)

venlafaxine hydrochloride (75 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": "4fb50561-0316-46fa-927e-4b33441de698", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["7852be9e-0c1d-47a8-9513-c3a04b365763"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-2180-0)", "package_ndc": "50090-2180-0", "marketing_start_date": "20151026"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-2180-1)", "package_ndc": "50090-2180-1", "marketing_start_date": "20151026"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "50090-2180_4fb50561-0316-46fa-927e-4b33441de698", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50090-2180", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20110601", "listing_expiration_date": "20261231"}