Furosemide
- Product NDC
- 23155-521
- 11-digit product format
- 231550521
- Labeler code
- 23155
- Product ID
- 23155-521_3b918f05-7bc3-4727-bcd0-d6c718b6efe7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Heritage Pharmaceuticals Inc.
- Application
- ANDA203428
- Marketing category
- ANDA
- Marketing start
- 2015-06-26
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 23155-521-31 | ML - Milliliter | 23155-521 | 047824b0-1fe8-45a7-a3d2-accc86149176 | 1 | 2015-08-04 |
| 23155-521-32 | ML - Milliliter | 23155-521 | 5d83eefd-cbf1-4ca7-b69b-bd5651eddda2 | 1 | 2015-08-04 |
| 23155-521-33 | ML - Milliliter | 23155-521 | 543be641-6be6-4079-9bad-e656c50eaad4 | 1 | 2015-08-04 |
| 23155-521-41 | ML - Milliliter | 23155-521 | b7b90f1a-1ee9-4c55-94ae-1234551cfb1d | 1 | 2015-08-04 |
| 23155-521-42 | ML - Milliliter | 23155-521 | 36444026-bf8c-4c02-b4e1-b2e9d58b3c63 | 1 | 2015-08-04 |
| 23155-521-44 | ML - Milliliter | 23155-521 | edb5fa0c-2404-4621-83be-e8136acc618c | 1 | 2015-08-04 |