Fludrocortisone Acetate
- Product NDC
- 71335-2454
- 11-digit product format
- 713352454
- Labeler code
- 71335
- Product ID
- 71335-2454_e41b141d-6aec-4008-a178-83a517cebfff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fludrocortisone Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA215279
- Marketing category
- ANDA
- Marketing start
- 2022-06-02
- Substance
- FLUDROCORTISONE ACETATE
- Active strength
- .1 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
- Fludrocortisone Acetate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FLUDROCORTISONE ACETATE | .1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V47IF0PVH4 |
| Rxcui | 313979 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2454-1 | Fludrocortisone Acetate | 100 in 1 BOTTLE | TABLET | 100 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-2454 | FLUDROCORTISONE ACETATE TABLET [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20240731_3d6f1a89-ea11-474d-aaca-64fea02a3beb.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2454-1 | 71335245401 | 100 TABLET in 1 BOTTLE (71335-2454-1) | 100 tablet | 2024-07-30 | No | No | Current |