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 150 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6896
Product ID 50090-6896_0b64f645-6a4f-453e-931f-f4f0cae3c669
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200834
Listing Expiration 2026-12-31
Marketing Start 2011-11-23

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 500906896
Hyphenated Format 50090-6896

Supplemental Identifiers

RxCUI
313581
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
  • 150 mg/1
source: ndc
Packaging
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-6896-0)
source: ndc

Packages (1)

50090-6896-0 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-6896-0)

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": "0b64f645-6a4f-453e-931f-f4f0cae3c669", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581"], "spl_set_id": ["296d6ab7-8c0c-40e5-8cb2-9d125b42b8bb"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-6896-0)", "package_ndc": "50090-6896-0", "marketing_start_date": "20231211"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "50090-6896_0b64f645-6a4f-453e-931f-f4f0cae3c669", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50090-6896", "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": "150 mg/1"}], "application_number": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20111123", "listing_expiration_date": "20261231"}