Fludrocortisone Acetate
- Product NDC
- 72603-170
- 11-digit product format
- 726030170
- Labeler code
- 72603
- Product ID
- 72603-170_04ad6ba3-6782-b5df-e063-6294a90a7e6e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fludrocortisone Acetate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NorthStar Rx LLC
- Application
- ANDA215279
- Marketing category
- ANDA
- Marketing start
- 2023-09-07
- 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 |
|---|
| 72603-170-01 | Fludrocortisone Acetate | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72603-170 | FLUDROCORTISONE ACETATE TABLET [NORTHSTAR RX LLC] | 1 | Current NDC, 1 package rows | 20230914_04ad6ba3-6781-b5df-e063-6294a90a7e6e.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 |
|---|
| 72603-170-01 | 72603017001 | 100 TABLET in 1 BOTTLE (72603-170-01) | 100 tablet | 2023-09-07 | No | No | Historical |