Furosemide
- Product NDC
- 50090-3262
- 11-digit product format
- 500903262
- Labeler code
- 50090
- Product ID
- 50090-3262_338158cb-a79e-4562-adcf-fa9de8fc3f1a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA018823
- Marketing category
- NDA
- Marketing start
- 1983-11-10
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-3262-0 | Furosemide | 30 in 1 BOTTLE | TABLET | 30 | | 14 |
| 50090-3262-1 | Furosemide | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 14 |
| 50090-3262-3 | Furosemide | 60 in 1 BOTTLE, PLASTIC | TABLET | 60 | | 14 |
| 50090-3262-9 | Furosemide | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 14 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3262 | FUROSEMIDE TABLET [A-S MEDICATION SOLUTIONS] | 14 | Legacy NDC, 4 package rows | 20210615_0a9a73b7-5717-40e8-9143-84c3b9d3053f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-3262-0 | 50090326200 | 30 in 1 BOTTLE | Historical |
| 50090-3262-1 | 50090326201 | 100 in 1 BOTTLE, PLASTIC | Historical |
| 50090-3262-3 | 50090326203 | 60 in 1 BOTTLE, PLASTIC | Historical |
| 50090-3262-9 | 50090326209 | 90 in 1 BOTTLE, PLASTIC | Historical |