Fenofibric Acid
- Product NDC
- 69973-105
- 11-digit product format
- 699730105
- Labeler code
- 69973
- Product ID
- 69973-105_57620cb7-e168-4a65-a3fc-420bf17d3c58
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibric Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Halton Laboratories
- Application
- NDA022418
- Marketing category
- NDA
- Marketing start
- 2015-07-30
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRIC ACID
- Active strength
- 105 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69973-105-30 | Fenofibric Acid | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 5 |
| 69973-105-90 | Fenofibric Acid | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69973-105 | FENOFIBRIC ACID TABLET [HALTON LABORATORIES] | 5 | Legacy NDC, 2 package rows | 20181012_be471aad-d936-48be-8c79-351b56ae9cc7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 69973-105-30 | 69973010530 | 30 in 1 BOTTLE, PLASTIC | Historical |
| 69973-105-90 | 69973010590 | 90 in 1 BOTTLE, PLASTIC | Historical |