venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

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

Drug Facts

Product Profile

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

venlafaxine hydrochloride 150 mg/1

Manufacturer
Granules Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 70010-186
Product ID 70010-186_451b69d2-6ed2-bf1c-e063-6294a90ac3b5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217390
Listing Expiration 2026-12-31
Marketing Start 2023-09-25

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 70010186
Hyphenated Format 70010-186

Supplemental Identifiers

RxCUI
313581 313583 313585
UPC
0370010185036 0370010184039 0370010186033
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 ANDA217390 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-186-03)
  • 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-186-05)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-186-09)
  • 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-186-10)
source: ndc

Packages (4)

70010-186-03 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-186-03) 70010-186-05 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-186-05) 70010-186-09 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-186-09) 70010-186-10 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-186-10)

Ingredients (1)

venlafaxine hydrochloride (150 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": "451b69d2-6ed2-bf1c-e063-6294a90ac3b5", "openfda": {"upc": ["0370010185036", "0370010184039", "0370010186033"], "unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["67059969-e291-4609-b130-0faacf2a19f0"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-186-03)", "package_ndc": "70010-186-03", "marketing_start_date": "20230925"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-186-05)", "package_ndc": "70010-186-05", "marketing_start_date": "20230925"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-186-09)", "package_ndc": "70010-186-09", "marketing_start_date": "20230925"}, {"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-186-10)", "package_ndc": "70010-186-10", "marketing_start_date": "20240509"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "70010-186_451b69d2-6ed2-bf1c-e063-6294a90ac3b5", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70010-186", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Granules Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA217390", "marketing_category": "ANDA", "marketing_start_date": "20230925", "listing_expiration_date": "20261231"}