vizimpro

Generic: dacomitinib

Labeler: pfizer laboratories div pfizer inc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name vizimpro
Generic Name dacomitinib
Labeler pfizer laboratories div pfizer inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

dacomitinib 15 mg/1

Manufacturer
Pfizer Laboratories Div Pfizer Inc

Identifiers & Regulatory

Product NDC 0069-0197
Product ID 0069-0197_cf672c83-c9d9-4107-bcf1-76d4106537cc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA211288
Listing Expiration 2026-12-31
Marketing Start 2018-10-04

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00690197
Hyphenated Format 0069-0197

Supplemental Identifiers

RxCUI
2058915 2058922 2058924 2058926 2058930 2058932
UPC
0300691198308 0300692299301 0300690197302
UNII
5092U85G58

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 vizimpro (source: ndc)
Generic Name dacomitinib (source: ndc)
Application Number NDA211288 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0069-0197-30)
source: ndc

Packages (1)

0069-0197-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0069-0197-30)

Ingredients (1)

dacomitinib (15 mg/1)

Linked Drug Pages (1)

Vizimpro ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cf672c83-c9d9-4107-bcf1-76d4106537cc", "openfda": {"upc": ["0300691198308", "0300692299301", "0300690197302"], "unii": ["5092U85G58"], "rxcui": ["2058915", "2058922", "2058924", "2058926", "2058930", "2058932"], "spl_set_id": ["4ab27d2f-e385-4e9c-b324-fa69c10b855a"], "manufacturer_name": ["Pfizer Laboratories Div Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0069-0197-30)", "package_ndc": "0069-0197-30", "marketing_start_date": "20181004"}], "brand_name": "Vizimpro", "product_id": "0069-0197_cf672c83-c9d9-4107-bcf1-76d4106537cc", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0069-0197", "generic_name": "dacomitinib", "labeler_name": "Pfizer Laboratories Div Pfizer Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vizimpro", "active_ingredients": [{"name": "DACOMITINIB", "strength": "15 mg/1"}], "application_number": "NDA211288", "marketing_category": "NDA", "marketing_start_date": "20181004", "listing_expiration_date": "20261231"}