venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

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

Drug Facts

Product Profile

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

venlafaxine hydrochloride 150 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2259
Product ID 70518-2259_49ef8066-9ca5-1d82-e063-6394a90a74a5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200834
Listing Expiration 2027-12-31
Marketing Start 2019-08-09

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 705182259
Hyphenated Format 70518-2259

Supplemental Identifiers

RxCUI
313581
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 ANDA200834 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2259-1)
  • 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-2259-2)
  • 30 POUCH in 1 BOX (70518-2259-5) / 1 CAPSULE, EXTENDED RELEASE in 1 POUCH (70518-2259-6)
source: ndc

Packages (3)

70518-2259-1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2259-1) 70518-2259-2 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-2259-2) 70518-2259-5 30 POUCH in 1 BOX (70518-2259-5) / 1 CAPSULE, EXTENDED RELEASE in 1 POUCH (70518-2259-6)

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": "49ef8066-9ca5-1d82-e063-6394a90a74a5", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581"], "spl_set_id": ["50d3b487-9f65-4e2f-b6eb-9533964f8972"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2259-1)", "package_ndc": "70518-2259-1", "marketing_start_date": "20200819"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-2259-2)", "package_ndc": "70518-2259-2", "marketing_start_date": "20201102"}, {"sample": false, "description": "30 POUCH in 1 BOX (70518-2259-5)  / 1 CAPSULE, EXTENDED RELEASE in 1 POUCH (70518-2259-6)", "package_ndc": "70518-2259-5", "marketing_start_date": "20230828"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "70518-2259_49ef8066-9ca5-1d82-e063-6394a90a74a5", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-2259", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20190809", "listing_expiration_date": "20271231"}