Furosemide
- Product NDC
- 63739-541
- 11-digit product format
- 637390541
- Labeler code
- 63739
- Product ID
- 63739-541_ba8af2d9-c523-4e7b-84c9-120cc6c52cdf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA078010
- Marketing category
- ANDA
- Marketing start
- 2011-08-22
- Marketing end
- 0000-00-00
- Substance
- FUROSEMIDE
- Active strength
- 20 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
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63739-541-01 | 2020-07-22 | C162847 | 48780-1 | ab0e2407-2642-f274-e053-dbdaa90a6471 | f3144b19-e282-4cde-82ad-c6ff69ba07cd |
| 63739-541-04 | 2020-07-22 | C162847 | 48780-1 | ab0e2407-2642-f274-e053-dbdaa90a6471 | f3144b19-e282-4cde-82ad-c6ff69ba07cd |
| 63739-541-10 | 2020-07-22 | C162847 | 48780-1 | ab0e2407-2642-f274-e053-dbdaa90a6471 | f3144b19-e282-4cde-82ad-c6ff69ba07cd |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63739-541-01 | EA - Each | 63739-541 | 4609cf9f-be64-4b71-a674-b575a2eab30a | 1 | 2012-07-24 |
| 63739-541-04 | EA - Each | 63739-541 | 68fffb21-6aef-44d3-b2c6-c1b778ff6cf9 | 1 | 2012-07-24 |
| 63739-541-10 | EA - Each | 63739-541 | 583f1c16-ef5e-4676-86fa-b4b154316ec7 | 1 | 2012-07-24 |