Furosemide
- Product NDC
- 50090-0150
- 11-digit product format
- 500900150
- Labeler code
- 50090
- Product ID
- 50090-0150_7b276796-d7d4-410c-b373-6adebd1a3467
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA018569
- Marketing category
- NDA
- Marketing start
- 1981-10-19
- Marketing end
- 0000-00-00
- Substance
- FUROSEMIDE
- Active strength
- 80 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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-0150-0 | Furosemide | 100 in 1 BOTTLE | TABLET | 100 | | 13 |
| 50090-0150-1 | Furosemide | 30 in 1 BOTTLE | TABLET | 30 | | 13 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-0150 | FUROSEMIDE TABLET [A-S MEDICATION SOLUTIONS] | 13 | Legacy NDC, 2 package rows | 20190329_b0115c7b-48e6-4a8c-8e35-52a757cadfac.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0150-0 | 50090015000 | 100 TABLET in 1 BOTTLE (50090-0150-0) | 100 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0150-1 | 50090015001 | 30 in 1 BOTTLE | | | | | | Historical |