Furosemide
- Product NDC
- 63629-1434
- 11-digit product format
- 636291434
- Labeler code
- 63629
- Product ID
- 63629-1434_39b5849c-2278-47dd-9eee-f65580174ffe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078010
- Marketing category
- ANDA
- Marketing start
- 2009-01-29
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63629-1434-1 | EA - Each | 63629-1434 | 5ae1e43f-dfbd-4f59-99b9-200b377e7882 | 1 | 2012-07-24 |
| 63629-1434-2 | EA - Each | 63629-1434 | 45b5e0d6-a387-4119-818a-4b8ff373e890 | 1 | 2012-07-24 |
| 63629-1434-3 | EA - Each | 63629-1434 | af0fc6a8-741d-408e-a871-ebc6dec9ac60 | 1 | 2012-07-24 |
| 63629-1434-4 | EA - Each | 63629-1434 | 319ee86a-9c5c-4b4d-bfb0-aefd9edfe814 | 1 | 2013-02-13 |
| 63629-1434-5 | EA - Each | 63629-1434 | 031fd03e-44b3-42fe-a943-4d8ea301c0e0 | 1 | 2013-02-13 |
| 63629-1434-6 | EA - Each | 63629-1434 | c8418a56-1028-4b5d-b39f-01e02abd5880 | 1 | 2013-02-13 |
| 63629-1434-7 | EA - Each | 63629-1434 | 0caddc62-b23b-45ff-a69d-157dc9c045e4 | 1 | 2013-02-13 |