venlafaxine

Generic: venlafaxine hydrochloride

Labeler: st. mary's medical park pharmacy
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

venlafaxine hydrochloride 37.5 mg/1

Manufacturer
St. Mary's Medical Park Pharmacy

Identifiers & Regulatory

Product NDC 60760-187
Product ID 60760-187_8a1e6dab-5331-1ea4-e053-2a95a90a0e40
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090555
Listing Expiration 2026-12-31
Marketing Start 2019-05-29

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 60760187
Hyphenated Format 60760-187

Supplemental Identifiers

RxCUI
313584
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 hydrochloride (source: ndc)
Application Number ANDA090555 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE, PLASTIC (60760-187-60)
source: ndc

Packages (1)

60760-187-60 60 TABLET in 1 BOTTLE, PLASTIC (60760-187-60)

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": "8a1e6dab-5331-1ea4-e053-2a95a90a0e40", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313584"], "spl_set_id": ["8a1e6dab-5330-1ea4-e053-2a95a90a0e40"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (60760-187-60)", "package_ndc": "60760-187-60", "marketing_start_date": "20190529"}], "brand_name": "venlafaxine", "product_id": "60760-187_8a1e6dab-5331-1ea4-e053-2a95a90a0e40", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "60760-187", "generic_name": "venlafaxine hydrochloride", "labeler_name": "St. Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA090555", "marketing_category": "ANDA", "marketing_start_date": "20190529", "listing_expiration_date": "20261231"}