pentoxifylline

Generic: pentoxifylline

Labeler: ncs healthcare of ky, llc dba vangard labs
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pentoxifylline
Generic Name pentoxifylline
Labeler ncs healthcare of ky, llc dba vangard labs
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

pentoxifylline 400 mg/1

Manufacturer
NCS HealthCare of KY, LLC dba Vangard Labs

Identifiers & Regulatory

Product NDC 0615-8511
Product ID 0615-8511_e3966eca-d995-479b-b2a3-4fd6eea51cb1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074878
Listing Expiration 2026-12-31
Marketing Start 2024-01-15

Pharmacologic Class

Established (EPC)
blood viscosity reducer [epc]
Physiologic Effect
hematologic activity alteration [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 06158511
Hyphenated Format 0615-8511

Supplemental Identifiers

RxCUI
312301
UNII
SD6QCT3TSU
NUI
N0000175895 N0000009065

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 pentoxifylline (source: ndc)
Generic Name pentoxifylline (source: ndc)
Application Number ANDA074878 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8511-39)
source: ndc

Packages (1)

0615-8511-39 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8511-39)

Ingredients (1)

pentoxifylline (400 mg/1)

Linked Drug Pages (1)

Pentoxifylline ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e3966eca-d995-479b-b2a3-4fd6eea51cb1", "openfda": {"nui": ["N0000175895", "N0000009065"], "unii": ["SD6QCT3TSU"], "rxcui": ["312301"], "spl_set_id": ["bd2f2672-62cd-4e77-8b0b-782f5d06198b"], "pharm_class_pe": ["Hematologic Activity Alteration [PE]"], "pharm_class_epc": ["Blood Viscosity Reducer [EPC]"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8511-39)", "package_ndc": "0615-8511-39", "marketing_start_date": "20240626"}], "brand_name": "Pentoxifylline", "product_id": "0615-8511_e3966eca-d995-479b-b2a3-4fd6eea51cb1", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Blood Viscosity Reducer [EPC]", "Hematologic Activity Alteration [PE]"], "product_ndc": "0615-8511", "generic_name": "Pentoxifylline", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pentoxifylline", "active_ingredients": [{"name": "PENTOXIFYLLINE", "strength": "400 mg/1"}], "application_number": "ANDA074878", "marketing_category": "ANDA", "marketing_start_date": "20240115", "listing_expiration_date": "20261231"}