venlafaxine

Generic: venlafaxine

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

Drug Facts

Product Profile

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

venlafaxine hydrochloride 50 mg/1

Manufacturer
Alembic Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 46708-432
Product ID 46708-432_47576e3f-2b6d-4334-8733-748687e5b784
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 46708432
Hyphenated Format 46708-432

Supplemental Identifiers

RxCUI
313580 313582 313584 313586 314277
UPC
0346708433307 0346708434304 0346708431303 0346708432300 0346708430306
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
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (46708-432-30)
  • 100 TABLET in 1 BOTTLE (46708-432-31)
  • 1000 TABLET in 1 BOTTLE (46708-432-91)
source: ndc

Packages (3)

46708-432-30 30 TABLET in 1 BOTTLE (46708-432-30) 46708-432-31 100 TABLET in 1 BOTTLE (46708-432-31) 46708-432-91 1000 TABLET in 1 BOTTLE (46708-432-91)

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": "47576e3f-2b6d-4334-8733-748687e5b784", "openfda": {"upc": ["0346708433307", "0346708434304", "0346708431303", "0346708432300", "0346708430306"], "unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["b73da6e2-1494-436f-a204-2e4e4c5974b6"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (46708-432-30)", "package_ndc": "46708-432-30", "marketing_start_date": "20151001"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (46708-432-31)", "package_ndc": "46708-432-31", "marketing_start_date": "20151001"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (46708-432-91)", "package_ndc": "46708-432-91", "marketing_start_date": "20151001"}], "brand_name": "venlafaxine", "product_id": "46708-432_47576e3f-2b6d-4334-8733-748687e5b784", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "46708-432", "generic_name": "venlafaxine", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA078932", "marketing_category": "ANDA", "marketing_start_date": "20151001", "listing_expiration_date": "20261231"}