Furosemide
- Product NDC
- 53217-182
- 11-digit product format
- 532170182
- Labeler code
- 53217
- Product ID
- 53217-182_53f94619-b9c5-4655-93ef-d5a409557b55
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA077293
- Marketing category
- ANDA
- Marketing start
- 2006-02-01
- Marketing end
- 0000-00-00
- Substance
- FUROSEMIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE],Loop Diuretic [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 |
|---|
| 53217-182-00 | Furosemide | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
| 53217-182-30 | Furosemide | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
| 53217-182-60 | Furosemide | 60 in 1 BOTTLE | TABLET | 60 | | 3 |
| 53217-182-90 | Furosemide | 90 in 1 BOTTLE | TABLET | 90 | | 3 |
| 53217-182-99 | Furosemide | 180 in 1 BOTTLE | TABLET | 180 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53217-182 | FUROSEMIDE TABLET [AIDAREX PHARMACEUTICALS LLC] | 3 | Legacy NDC, 5 package rows | 20170413_e44cc8ac-1e04-4910-bde1-1f4a45a6937f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53217-182-00 | 53217018200 | 100 in 1 BOTTLE | Historical |
| 53217-182-30 | 53217018230 | 30 in 1 BOTTLE | Historical |
| 53217-182-60 | 53217018260 | 60 in 1 BOTTLE | Historical |
| 53217-182-90 | 53217018290 | 90 in 1 BOTTLE | Historical |
| 53217-182-99 | 53217018299 | 180 in 1 BOTTLE | Historical |