Furosemide
- Product NDC
- 67046-228
- 11-digit product format
- 670460228
- Labeler code
- 67046
- Product ID
- 67046-228_1d44526e-563e-4cd2-9625-983d8c31a434
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- ANDA078010
- Marketing category
- ANDA
- Marketing start
- 2011-05-01
- 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
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 67046-228-30 | Furosemide | 30 in 1 BLISTER PACK | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67046-228 | FUROSEMIDE TABLET [CONTRACT PHARMACY SERVICES-PA] | 1 | Legacy NDC, 1 package rows | 20111206_1d44526e-563e-4cd2-9625-983d8c31a434.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 67046-228-30 | 67046022830 | 30 in 1 BLISTER PACK | Historical |