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, COATED
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 75 mg/1

Manufacturer
Cadila Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 71209-087
Product ID 71209-087_5e8d05f3-2a6f-4132-b7e3-9dc90804f2d3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211323
Listing Expiration 2026-12-31
Marketing Start 2018-01-05

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 71209087
Hyphenated Format 71209-087

Supplemental Identifiers

RxCUI
808744 808748 808753
UPC
0371209087117 0371209089111
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 ANDA211323 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 30 TABLET, COATED in 1 BOTTLE (71209-087-01)
  • 90 TABLET, COATED in 1 BOTTLE (71209-087-04)
  • 1000 TABLET, COATED in 1 BOTTLE (71209-087-11)
source: ndc

Packages (3)

71209-087-01 30 TABLET, COATED in 1 BOTTLE (71209-087-01) 71209-087-04 90 TABLET, COATED in 1 BOTTLE (71209-087-04) 71209-087-11 1000 TABLET, COATED in 1 BOTTLE (71209-087-11)

Ingredients (1)

venlafaxine hydrochloride (75 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": "5e8d05f3-2a6f-4132-b7e3-9dc90804f2d3", "openfda": {"upc": ["0371209087117", "0371209089111"], "unii": ["7D7RX5A8MO"], "rxcui": ["808744", "808748", "808753"], "spl_set_id": ["516e7566-35c2-4a25-88d8-54d9dbc8f6be"], "manufacturer_name": ["Cadila Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (71209-087-01)", "package_ndc": "71209-087-01", "marketing_start_date": "20180816"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (71209-087-04)", "package_ndc": "71209-087-04", "marketing_start_date": "20180816"}, {"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (71209-087-11)", "package_ndc": "71209-087-11", "marketing_start_date": "20180816"}], "brand_name": "Venlafaxine", "product_id": "71209-087_5e8d05f3-2a6f-4132-b7e3-9dc90804f2d3", "dosage_form": "TABLET, COATED", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "71209-087", "generic_name": "Venlafaxine", "labeler_name": "Cadila Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA211323", "marketing_category": "ANDA", "marketing_start_date": "20180105", "listing_expiration_date": "20261231"}