venlafaxine

Generic: venlafaxine hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine
Generic Name venlafaxine hydrochloride
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 50 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-1907
Product ID 70518-1907_49887040-f479-936a-e063-6294a90a9bef
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090555
Listing Expiration 2027-12-31
Marketing Start 2019-02-25

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 705181907
Hyphenated Format 70518-1907

Supplemental Identifiers

RxCUI
314277
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 (source: ndc)
Generic Name venlafaxine hydrochloride (source: ndc)
Application Number ANDA090555 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-1907-0)
source: ndc

Packages (1)

70518-1907-0 30 TABLET in 1 BLISTER PACK (70518-1907-0)

Ingredients (1)

venlafaxine hydrochloride (50 mg/1)

Linked Drug Pages (1)

venlafaxine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49887040-f479-936a-e063-6294a90a9bef", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["314277"], "spl_set_id": ["b19ec628-4034-4316-ad3d-46c1ee220728"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-1907-0)", "package_ndc": "70518-1907-0", "marketing_start_date": "20190225"}], "brand_name": "venlafaxine", "product_id": "70518-1907_49887040-f479-936a-e063-6294a90a9bef", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-1907", "generic_name": "venlafaxine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA090555", "marketing_category": "ANDA", "marketing_start_date": "20190225", "listing_expiration_date": "20271231"}