venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

Labeler: st. marys medical park pharmacy
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler st. marys medical park pharmacy
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 75 mg/1

Manufacturer
St. Marys Medical Park Pharmacy

Identifiers & Regulatory

Product NDC 60760-121
Product ID 60760-121_ef538879-d19d-4f2b-e053-2995a90a4588
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077653
Listing Expiration 2026-12-31
Marketing Start 2011-01-30

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 60760121
Hyphenated Format 60760-121

Supplemental Identifiers

RxCUI
313586
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 hydrochloride (source: ndc)
Generic Name venlafaxine hydrochloride (source: ndc)
Application Number ANDA077653 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (60760-121-30)
source: ndc

Packages (1)

60760-121-30 30 TABLET in 1 BOTTLE, PLASTIC (60760-121-30)

Ingredients (1)

venlafaxine hydrochloride (75 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": "ef538879-d19d-4f2b-e053-2995a90a4588", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313586"], "spl_set_id": ["341720f7-f76f-498b-856f-3d207ad63feb"], "manufacturer_name": ["St. Marys Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (60760-121-30)", "package_ndc": "60760-121-30", "marketing_start_date": "20110130"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "60760-121_ef538879-d19d-4f2b-e053-2995a90a4588", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "60760-121", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "St. Marys Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA077653", "marketing_category": "ANDA", "marketing_start_date": "20110130", "listing_expiration_date": "20261231"}