Furosemide
- Product NDC
- 62135-754
- 11-digit product format
- 621350754
- Labeler code
- 62135
- Product ID
- 62135-754_31443d9b-3dee-5aa9-e063-6294a90adcfd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- NDA018413
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1983-11-30
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Furosemide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FUROSEMIDE | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7LXU5N7ZO5 |
| Rxcui | 310429, 313988 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62135-754-90 | Furosemide | 90 in 1 PACKAGE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-754 | FUROSEMIDE TABLET [CHARTWELL RX, LLC] | 2 | Current NDC, 1 package rows | 20250328_8ebd2f10-acfc-48a4-a5db-f20377bda9ce.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 62135-754-90 | 62135075490 | 90 TABLET in 1 PACKAGE (62135-754-90) | 90 tablet | 2024-04-17 | No | No | Historical |