venlafaxine

Generic: venlafaxine

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine
Generic Name venlafaxine
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 75 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-633
Product ID 43063-633_4139d5c9-2e2b-7f2d-e063-6394a90a35e6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078627
Listing Expiration 2026-12-31
Marketing Start 2008-06-13

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 43063633
Hyphenated Format 43063-633

Supplemental Identifiers

RxCUI
313586
UPC
0343063633908
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 (source: ndc)
Application Number ANDA078627 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE, PLASTIC (43063-633-90)
source: ndc

Packages (1)

43063-633-90 90 TABLET in 1 BOTTLE, PLASTIC (43063-633-90)

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": "4139d5c9-2e2b-7f2d-e063-6394a90a35e6", "openfda": {"upc": ["0343063633908"], "unii": ["7D7RX5A8MO"], "rxcui": ["313586"], "spl_set_id": ["18495527-add4-42a5-bbf7-9f8dc2df06af"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-633-90)", "package_ndc": "43063-633-90", "marketing_start_date": "20151125"}], "brand_name": "Venlafaxine", "product_id": "43063-633_4139d5c9-2e2b-7f2d-e063-6394a90a35e6", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "43063-633", "generic_name": "Venlafaxine", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA078627", "marketing_category": "ANDA", "marketing_start_date": "20080613", "listing_expiration_date": "20261231"}