venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

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

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler alembic pharmaceuticals inc.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 37.5 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-792
Product ID 62332-792_66ab68e0-e9f1-4576-8a95-6bbe3682fd9b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217767
Listing Expiration 2026-12-31
Marketing Start 2024-06-10

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 62332792
Hyphenated Format 62332-792

Supplemental Identifiers

RxCUI
313581 313583 313585
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 ANDA217767 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 37.5 mg/1
source: ndc
Packaging
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-792-30)
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-792-31)
  • 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-792-71)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-792-90)
  • 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-792-91)
source: ndc

Packages (5)

62332-792-30 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-792-30) 62332-792-31 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-792-31) 62332-792-71 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-792-71) 62332-792-90 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-792-90) 62332-792-91 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-792-91)

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": "66ab68e0-e9f1-4576-8a95-6bbe3682fd9b", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["5c943206-6df8-4fc5-ab1d-d34b9715182c"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-792-30)", "package_ndc": "62332-792-30", "marketing_start_date": "20240610"}, {"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-792-31)", "package_ndc": "62332-792-31", "marketing_start_date": "20240610"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-792-71)", "package_ndc": "62332-792-71", "marketing_start_date": "20240610"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-792-90)", "package_ndc": "62332-792-90", "marketing_start_date": "20240610"}, {"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-792-91)", "package_ndc": "62332-792-91", "marketing_start_date": "20240610"}], "brand_name": "VENLAFAXINE HYDROCHLORIDE", "product_id": "62332-792_66ab68e0-e9f1-4576-8a95-6bbe3682fd9b", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "62332-792", "generic_name": "VENLAFAXINE HYDROCHLORIDE", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VENLAFAXINE HYDROCHLORIDE", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA217767", "marketing_category": "ANDA", "marketing_start_date": "20240610", "listing_expiration_date": "20261231"}