FUROSEMIDE
- Product NDC
- 71872-7277
- 11-digit product format
- 718727277
- Labeler code
- 71872
- Product ID
- 71872-7277_d89f5657-1030-7a47-e053-2995a90aaf7a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA077941
- Marketing category
- ANDA
- Marketing start
- 2007-03-22
- Marketing end
- 0000-00-00
- Substance
- FUROSEMIDE
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71872-7277 | FUROSEMIDE INJECTION [MEDICAL PURCHASING SOLUTIONS, LLC] | 2 | Legacy NDC | 20230504_d89f49d5-e41a-ba14-e053-2995a90a0268.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71872-7277-1 | 71872727701 | 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7277-1) > 2 mL in 1 VIAL, SINGLE-DOSE | 2022-01-10 | 0000-00-00 | No | No | Current |