Furosemide
- Product NDC
- 64205-739
- 11-digit product format
- 642050739
- Labeler code
- 64205
- Product ID
- 64205-739_83abfca3-49a0-4f31-a4e4-ca3882f0021c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ReadyMeds
- Application
- ANDA076796
- Marketing category
- ANDA
- Marketing start
- 2004-03-26
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 64205-739-30 | Furosemide | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 9 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64205-739 | FUROSEMIDE TABLET [READYMEDS] | 9 | Legacy NDC, 1 package rows | 20140702_cfe67179-fbfe-402d-9326-07373bd93951.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64205-739-30 | 64205073930 | 30 in 1 BOTTLE, PLASTIC | Historical |