Posaconazole
- Product NDC
- 71335-2930
- 11-digit product format
- 713352930
- Labeler code
- 71335
- Product ID
- 71335-2930_aa780d7b-d64f-4642-8096-a4a9e474c356
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Posaconazole
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA216488
- Marketing category
- ANDA
- Marketing start
- 2023-09-15
- 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 |
|---|
| 71335-2930-1 | Posaconazole | 60 in 1 BOTTLE | TABLET, DELAYED RELEASE | 60 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2930-1 | 71335293001 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2930-1) | 2025-11-11 | No | No | Current |