venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

Labeler: yaopharma co., ltd.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler yaopharma co., ltd.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 37.5 mg/1

Manufacturer
Yaopharma Co., Ltd.

Identifiers & Regulatory

Product NDC 50771-002
Product ID 50771-002_4502de86-571d-cfb3-e063-6294a90a34f8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202036
Listing Expiration 2026-12-31
Marketing Start 2016-09-06

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 50771002
Hyphenated Format 50771-002

Supplemental Identifiers

RxCUI
313580 313582 313584 313586 314277
UPC
0350771003022 0350771002025 0350771001028 0350771004029
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 hydrochloride (source: ndc)
Generic Name venlafaxine hydrochloride (source: ndc)
Application Number ANDA202036 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (50771-002-02)
source: ndc

Packages (1)

50771-002-02 100 TABLET in 1 BOTTLE, PLASTIC (50771-002-02)

Ingredients (1)

venlafaxine hydrochloride (37.5 mg/1)

Linked Drug Pages (1)

Venlafaxine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4502de86-571d-cfb3-e063-6294a90a34f8", "openfda": {"upc": ["0350771003022", "0350771002025", "0350771001028", "0350771004029"], "unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["38fd2c97-cd30-2f7d-e054-00144ff8d46c"], "manufacturer_name": ["Yaopharma Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (50771-002-02)", "package_ndc": "50771-002-02", "marketing_start_date": "20160906"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "50771-002_4502de86-571d-cfb3-e063-6294a90a34f8", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50771-002", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Yaopharma Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA202036", "marketing_category": "ANDA", "marketing_start_date": "20160906", "listing_expiration_date": "20261231"}