Furosemide
- Product NDC
- 43063-075
- 11-digit product format
- 430630075
- Labeler code
- 43063
- Product ID
- 43063-075_7c4889dd-29cf-f1ec-e053-2991aa0a0e0c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA077293
- Marketing category
- ANDA
- Marketing start
- 2006-02-01
- 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
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 43063-075-01 | EA - Each | 43063-075 | b683194b-5bff-484d-a879-b7d7b281b5a8 | 1 | 2013-03-03 |
| 43063-075-04 | EA - Each | 43063-075 | 180cac00-e923-418b-b274-c0079e56ed2b | 1 | 2013-03-03 |
| 43063-075-10 | EA - Each | 43063-075 | e75b96c3-59b3-46b8-a2dd-151f25f23309 | 1 | 2013-05-02 |
| 43063-075-14 | EA - Each | 43063-075 | 33ab1150-76ed-4796-bd90-480fc400d1f8 | 1 | 2013-05-02 |
| 43063-075-30 | EA - Each | 43063-075 | 980218b0-bbd3-41d8-8d05-0bb389a3ec7d | 1 | 2013-05-02 |
| 43063-075-60 | EA - Each | 43063-075 | bbcae08d-adc0-452f-92a5-c731798d806d | 1 | 2013-05-02 |
| 43063-075-90 | EA - Each | 43063-075 | a83c404e-c858-4018-b294-ee4e7e93ea3b | 1 | 2013-03-03 |