Vizimpro
- Product NDC
- 0069-2299
- 11-digit product format
- 000692299
- Labeler code
- 0069
- Product ID
- 0069-2299_cf672c83-c9d9-4107-bcf1-76d4106537cc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dacomitinib
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Pfizer Laboratories Div Pfizer Inc
- Application
- NDA211288
- Marketing category
- NDA
- Marketing start
- 2018-10-04
- Substance
- DACOMITINIB
- Active strength
- 45 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Vizimpro
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DACOMITINIB | 45 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5092U85G58 |
| Rxcui | 2058915, 2058922, 2058924, 2058926, 2058930, 2058932 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0069-2299-30 | Vizimpro | 30 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 30 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0069-2299 | VIZIMPRO (DACOMITINIB) TABLET, FILM COATED [PFIZER LABORATORIES DIV PFIZER INC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20250119_4ab27d2f-e385-4e9c-b324-fa69c10b855a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0069-2299-30 | 00069229930 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0069-2299-30) | 2018-10-04 | 0000-00-00 | No | No | Current |