venlafaxine

Generic: venlafaxine

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

Drug Facts

Product Profile

Brand Name venlafaxine
Generic Name venlafaxine
Labeler alembic pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 37.5 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-009
Product ID 62332-009_8724b94d-b3fd-4844-a7fe-2be7982cf8f5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078932
Listing Expiration 2026-12-31
Marketing Start 2015-10-01

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 62332009
Hyphenated Format 62332-009

Supplemental Identifiers

RxCUI
313580 313582 313584 313586 314277
UPC
0362332008308 0362332010301 0362332012305 0362332011308
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 ANDA078932 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (62332-009-30)
  • 100 TABLET in 1 BOTTLE (62332-009-31)
  • 1000 TABLET in 1 BOTTLE (62332-009-91)
source: ndc

Packages (3)

62332-009-30 30 TABLET in 1 BOTTLE (62332-009-30) 62332-009-31 100 TABLET in 1 BOTTLE (62332-009-31) 62332-009-91 1000 TABLET in 1 BOTTLE (62332-009-91)

Ingredients (1)

venlafaxine hydrochloride (37.5 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": "8724b94d-b3fd-4844-a7fe-2be7982cf8f5", "openfda": {"upc": ["0362332008308", "0362332010301", "0362332012305", "0362332011308"], "unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["67b323a7-a8c9-410f-bff0-0e515bef41a7"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (62332-009-30)", "package_ndc": "62332-009-30", "marketing_start_date": "20151001"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (62332-009-31)", "package_ndc": "62332-009-31", "marketing_start_date": "20151001"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62332-009-91)", "package_ndc": "62332-009-91", "marketing_start_date": "20151001"}], "brand_name": "venlafaxine", "product_id": "62332-009_8724b94d-b3fd-4844-a7fe-2be7982cf8f5", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "62332-009", "generic_name": "venlafaxine", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA078932", "marketing_category": "ANDA", "marketing_start_date": "20151001", "listing_expiration_date": "20261231"}