Furosemide
- Product NDC
- 71610-305
- 11-digit product format
- 716100305
- Labeler code
- 71610
- Product ID
- 71610-305_f0960a17-009b-4da4-b2cc-7851e22a2165
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA070086
- Marketing category
- ANDA
- Marketing start
- 1986-01-24
- 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 |
|---|
| 71610-305-60 | Furosemide | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 1 |
| 71610-305-80 | Furosemide | 180 in 1 BOTTLE, PLASTIC | TABLET | 180 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71610-305 | FUROSEMIDE TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] | 1 | Legacy NDC, 2 package rows | 20190817_a0dd45a3-4ae8-4301-8d6c-a20eac80cb2c.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 |
|---|
| 71610-305-60 | 71610030560 | 90 TABLET in 1 BOTTLE, PLASTIC (71610-305-60) | 90 tablet | 2019-07-16 | 0000-00-00 | No | No | Current |
| 71610-305-80 | 71610030580 | 180 TABLET in 1 BOTTLE, PLASTIC (71610-305-80) | 180 tablet | 2019-07-16 | 0000-00-00 | No | No | Current |