venlafaxine hydrochloride, extended release

Generic: venlafaxine hydrochloride, extended release

Labeler: edenbridge pharmaceuticals llc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride, extended release
Generic Name venlafaxine hydrochloride, extended release
Labeler edenbridge pharmaceuticals llc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 150 mg/1

Manufacturer
Edenbridge Pharmaceuticals LLC.

Identifiers & Regulatory

Product NDC 42799-962
Product ID 42799-962_a7958920-40c7-4038-8524-3f830555d345
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209193
Listing Expiration 2027-12-31
Marketing Start 2023-03-15

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 42799962
Hyphenated Format 42799-962

Supplemental Identifiers

RxCUI
808744 808748
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, extended release (source: ndc)
Generic Name venlafaxine hydrochloride, extended release (source: ndc)
Application Number ANDA209193 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (42799-962-01)
  • 90 TABLET in 1 BOTTLE (42799-962-02)
source: ndc

Packages (2)

42799-962-01 30 TABLET in 1 BOTTLE (42799-962-01) 42799-962-02 90 TABLET in 1 BOTTLE (42799-962-02)

Ingredients (1)

venlafaxine hydrochloride (150 mg/1)

Linked Drug Pages (1)

venlafaxine hydrochloride, extended release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a7958920-40c7-4038-8524-3f830555d345", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["808744", "808748"], "spl_set_id": ["38431a76-6185-4c17-994f-8278b6cd7510"], "manufacturer_name": ["Edenbridge Pharmaceuticals LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (42799-962-01)", "package_ndc": "42799-962-01", "marketing_start_date": "20230315"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (42799-962-02)", "package_ndc": "42799-962-02", "marketing_start_date": "20230315"}], "brand_name": "venlafaxine hydrochloride, extended release", "product_id": "42799-962_a7958920-40c7-4038-8524-3f830555d345", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "42799-962", "generic_name": "venlafaxine hydrochloride, extended release", "labeler_name": "Edenbridge Pharmaceuticals LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine hydrochloride, extended release", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA209193", "marketing_category": "ANDA", "marketing_start_date": "20230315", "listing_expiration_date": "20271231"}