venlafaxine

Generic: venlafaxine

Labeler: cadila pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine
Generic Name venlafaxine
Labeler cadila pharmaceuticals limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 50 mg/1

Manufacturer
Cadila Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 71209-027
Product ID 71209-027_f6bcbdd6-db09-4aeb-8eb0-6eadb8ebdeba
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206250
Listing Expiration 2026-12-31
Marketing Start 2018-12-03

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 71209027
Hyphenated Format 71209-027

Supplemental Identifiers

RxCUI
313580 313582 313584 313586 314277
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 (source: ndc)
Generic Name venlafaxine (source: ndc)
Application Number ANDA206250 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (71209-027-05)
source: ndc

Packages (1)

71209-027-05 100 TABLET in 1 BOTTLE (71209-027-05)

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": "f6bcbdd6-db09-4aeb-8eb0-6eadb8ebdeba", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["2ed61dcf-42e3-47cf-a607-459eef5fea98"], "manufacturer_name": ["Cadila Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71209-027-05)", "package_ndc": "71209-027-05", "marketing_start_date": "20181203"}], "brand_name": "VENLAFAXINE", "product_id": "71209-027_f6bcbdd6-db09-4aeb-8eb0-6eadb8ebdeba", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71209-027", "generic_name": "venlafaxine", "labeler_name": "Cadila Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VENLAFAXINE", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA206250", "marketing_category": "ANDA", "marketing_start_date": "20181203", "listing_expiration_date": "20261231"}