POSACONAZOLE
- Product NDC
- 51407-676
- 11-digit product format
- 514070676
- Labeler code
- 51407
- Product ID
- 51407-676_2eebdc24-23e7-4a3c-e063-6394a90a26c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- posaconazole
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA212226
- Marketing category
- ANDA
- Marketing start
- 2022-05-10
- Substance
- POSACONAZOLE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Azole Antifungal [EPC], Azoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- POSACONAZOLE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POSACONAZOLE | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6TK1G07BHZ |
| Rxcui | 1482908 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51407-676-60 | POSACONAZOLE | 60 in 1 BOTTLE | TABLET, DELAYED RELEASE | 60 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51407-676 | POSACONAZOLE TABLET, DELAYED RELEASE [GOLDEN STATE MEDICAL SUPPLY, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250411_e883b495-d7e7-6d58-e053-2a95a90a1cd3.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 |
|---|
| 51407-676-60 | 51407067660 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (51407-676-60) | 2022-09-12 | 0000-00-00 | No | No | Current |