Furosemide
- Product NDC
- 67296-2136
- 11-digit product format
- 672962136
- Labeler code
- 67296
- Product ID
- 67296-2136_4f790a18-4685-89e3-e063-6294a90ab1a0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Redpharm Drug
- Application
- ANDA216629
- Marketing category
- ANDA
- Marketing start
- 2022-11-05
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Furosemide
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FUROSEMIDE | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7LXU5N7ZO5 |
| Rxcui | 310429 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67296-2136-1 | 67296213601 | 3 TABLET in 1 BOTTLE (67296-2136-1) | 3 tablet | 2022-11-05 | No | No | Historical |
| 67296-2136-2 | 67296213602 | 6 TABLET in 1 BOTTLE (67296-2136-2) | 6 tablet | 2022-11-05 | No | No | Historical |
| 67296-2136-3 | 67296213603 | 30 TABLET in 1 BOTTLE (67296-2136-3) | 30 tablet | 2022-11-05 | No | No | Historical |
| 67296-2136-4 | 67296213604 | 7 TABLET in 1 BOTTLE (67296-2136-4) | 7 tablet | 2022-11-05 | No | No | Historical |
| 67296-2136-5 | 67296213605 | 5 TABLET in 1 BOTTLE (67296-2136-5) | 5 tablet | 2022-11-05 | No | No | Historical |