pentoxifylline

Generic: pentoxifylline

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

Drug Facts

Product Profile

Brand Name pentoxifylline
Generic Name pentoxifylline
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

pentoxifylline 400 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-4532
Product ID 68071-4532_1a909abe-99ac-0b35-e063-6394a90aac4a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075028
Listing Expiration 2026-12-31
Marketing Start 2014-08-22

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 680714532
Hyphenated Format 68071-4532

Supplemental Identifiers

RxCUI
312301
UPC
0368071453294
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 ANDA075028 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-4532-9)
source: ndc

Packages (1)

68071-4532-9 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-4532-9)

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": "1a909abe-99ac-0b35-e063-6394a90aac4a", "openfda": {"nui": ["N0000175895", "N0000009065"], "upc": ["0368071453294"], "unii": ["SD6QCT3TSU"], "rxcui": ["312301"], "spl_set_id": ["73a6351c-5a8d-abbf-e053-2991aa0a5382"], "pharm_class_pe": ["Hematologic Activity Alteration [PE]"], "pharm_class_epc": ["Blood Viscosity Reducer [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-4532-9)", "package_ndc": "68071-4532-9", "marketing_start_date": "20180817"}], "brand_name": "Pentoxifylline", "product_id": "68071-4532_1a909abe-99ac-0b35-e063-6394a90aac4a", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Blood Viscosity Reducer [EPC]", "Hematologic Activity Alteration [PE]"], "product_ndc": "68071-4532", "generic_name": "Pentoxifylline", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pentoxifylline", "active_ingredients": [{"name": "PENTOXIFYLLINE", "strength": "400 mg/1"}], "application_number": "ANDA075028", "marketing_category": "ANDA", "marketing_start_date": "20140822", "listing_expiration_date": "20261231"}