Furosemide
- Product NDC
- 21695-491
- 11-digit product format
- 216950491
- Labeler code
- 21695
- Product ID
- 21695-491_b116f624-85d5-472a-8209-c80eae8204a6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distirbutors Corp
- Application
- ANDA078010
- Marketing category
- ANDA
- Marketing start
- 2006-09-18
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| d80d3aff-3a63-4d7b-a2be-fd9388b04330 | Product name | 9 | 20250806 |
| 9061e89f-9c86-4196-b34b-886fc1673cc4 | Product name | 1 | 20140821 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 21695-491-00 | 2019-09-24 | C162847 | 48780-1 | 934fe258-4cc8-48b1-e053-8cdaa90a720a | FUROSEMIDE TABLETS, USP Rx only |
| 21695-491-30 | 2019-09-24 | C162847 | 48780-1 | 934fe258-4cc8-48b1-e053-8cdaa90a720a | FUROSEMIDE TABLETS, USP Rx only |
| 21695-491-90 | 2019-09-24 | C162847 | 48780-1 | 934fe258-4cc8-48b1-e053-8cdaa90a720a | FUROSEMIDE TABLETS, USP Rx only |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 21695-491-00 | Furosemide | 100 in 1 BOTTLE | TABLET | 100 | 3 | |
| 21695-491-30 | Furosemide | 30 in 1 BOTTLE | TABLET | 30 | 3 | |
| 21695-491-90 | Furosemide | 90 in 1 BOTTLE | TABLET | 90 | 3 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 21695-491-00 | EA - Each | 21695-491 | 70cba00c-a50f-4947-8edd-6ee4a51b13a6 | 1 | 2012-07-24 |
| 21695-491-30 | EA - Each | 21695-491 | 0f976602-42eb-4cda-a7eb-dddb309a073c | 1 | 2012-07-24 |
| 21695-491-90 | EA - Each | 21695-491 | e5c8aaec-3aa5-4cce-90d7-a88c098e8ac9 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Furosemide | ACTIVE INGREDIENT | 7LXU5N7ZO5 | FUROSEMIDE TABLET [REBEL DISTIRBUTORS CORP] | 3 | |
| Furosemide | ACTIVE MOIETY | 7LXU5N7ZO5 | FUROSEMIDE TABLET [REBEL DISTIRBUTORS CORP] | 3 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | FUROSEMIDE TABLET [REBEL DISTIRBUTORS CORP] | 3 | |
| magnesium stearate | INACTIVE INGREDIENT | 70097M6I30 | FUROSEMIDE TABLET [REBEL DISTIRBUTORS CORP] | 3 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | FUROSEMIDE TABLET [REBEL DISTIRBUTORS CORP] | 3 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | FUROSEMIDE TABLET [REBEL DISTIRBUTORS CORP] | 3 |
DailyMed Dashboard NDC Coverage#
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 310429 | furosemide 20 MG Oral Tablet | PSN | d562faea-2800-4ed6-9213-88f072e21134 | 3 |
| 313988 | furosemide 40 MG Oral Tablet | PSN | d562faea-2800-4ed6-9213-88f072e21134 | 3 |
| 310429 | furosemide 20 MG Oral Tablet | SCD | d562faea-2800-4ed6-9213-88f072e21134 | 3 |
| 313988 | furosemide 40 MG Oral Tablet | SCD | d562faea-2800-4ed6-9213-88f072e21134 | 3 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 21695-491-00 | 21695049100 | 100 in 1 BOTTLE | Historical |
| 21695-491-30 | 21695049130 | 30 in 1 BOTTLE | Historical |
| 21695-491-90 | 21695049190 | 90 in 1 BOTTLE | Historical |