venlafaxine hydrochloride (31722-003)

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride

Generic Name venlafaxine hydrochloride

Labeler camber pharmaceuticals, inc.

Dosage Form CAPSULE, EXTENDED RELEASE

Routes

ORAL

Active Ingredients

venlafaxine hydrochloride 75 mg/1

Manufacturer

Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-003

Product ID 31722-003_1eee52e9-dda9-0d36-e063-6394a90a905b

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA212277

Listing Expiration 2026-12-31

Marketing Start 2019-07-08

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 31722003

Hyphenated Format 31722-003

Supplemental Identifiers

RxCUI

313581 313583 313585

UPC

0331722004305 0331722002301 0331722003308

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 ANDA212277 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

75 mg/1

source: ndc

Packaging

10 BLISTER PACK in 1 CARTON (31722-003-01) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-003-05)
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-003-30)
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-003-90)

source: ndc

Packages (4)

31722-003-01 10 BLISTER PACK in 1 CARTON (31722-003-01) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK 31722-003-05 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-003-05) 31722-003-30 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-003-30) 31722-003-90 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-003-90)

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": "1eee52e9-dda9-0d36-e063-6394a90a905b", "openfda": {"upc": ["0331722004305", "0331722002301", "0331722003308"], "unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["0ee91447-2c23-4519-81cc-550b5416dd6b"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (31722-003-01)  / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "31722-003-01", "marketing_start_date": "20190708"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-003-05)", "package_ndc": "31722-003-05", "marketing_start_date": "20190708"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-003-30)", "package_ndc": "31722-003-30", "marketing_start_date": "20190708"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-003-90)", "package_ndc": "31722-003-90", "marketing_start_date": "20190708"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "31722-003_1eee52e9-dda9-0d36-e063-6394a90a905b", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "31722-003", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA212277", "marketing_category": "ANDA", "marketing_start_date": "20190708", "listing_expiration_date": "20261231"}