Prescription drug · ANDA
Furosemide NDC 71335-2319
Furosemide 20 mg/1 · Tablet · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71335-2319-0 | 7133523190071335231900 | 6 TABLET in 1 BOTTLE (71335-2319-0)Marketed from Jan 4, 2024 | |
| 71335-2319-1 | 7133523190171335231901 | 30 TABLET in 1 BOTTLE (71335-2319-1)Marketed from Jan 4, 2024 | |
| 71335-2319-2 | 7133523190271335231902 | 90 TABLET in 1 BOTTLE (71335-2319-2)Marketed from Jan 4, 2024 | |
| 71335-2319-3 | 7133523190371335231903 | 60 TABLET in 1 BOTTLE (71335-2319-3)Marketed from Jan 4, 2024 | |
| 71335-2319-4 | 7133523190471335231904 | 100 TABLET in 1 BOTTLE (71335-2319-4)Marketed from Jan 4, 2024 | |
| 71335-2319-5 | 7133523190571335231905 | 7 TABLET in 1 BOTTLE (71335-2319-5)Marketed from Jan 4, 2024 | |
| 71335-2319-6 | 7133523190671335231906 | 28 TABLET in 1 BOTTLE (71335-2319-6)Marketed from Jan 4, 2024 | |
| 71335-2319-7 | 7133523190771335231907 | 14 TABLET in 1 BOTTLE (71335-2319-7)Marketed from Jan 4, 2024 | |
| 71335-2319-8 | 7133523190871335231908 | 10 TABLET in 1 BOTTLE (71335-2319-8)Marketed from Jan 4, 2024 | |
| 71335-2319-9 | 7133523190971335231909 | 20 TABLET in 1 BOTTLE (71335-2319-9)Marketed from Jan 4, 2024 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Furosemide
- Generic name (nonproprietary)
- furosemide
- Active ingredients
- Furosemide — 20 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Bryant Ranch PrepackNDC labeler code 71335
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 216629
- Marketing start
- Listing expires
- Other FDA classes
- Increased Diuresis at Loop of Henle (Physiologic effect)
- Identifiers
- Product ID 71335-2319_bf3ea890-deb2-4839-9cfe-062f8afec109SPL ID bf3ea890-deb2-4839-9cfe-062f8afec109SPL set ID 53c3f50f-57c6-441b-afea-ec43d7943d1aRxCUI 310429UNII 7LXU5N7ZO5
- Pharmacologic class
- Loop Diuretic
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N471335231900followed by a unit qualifier and the quantityPackage 71335-2319-00. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATIONS AND USAGE Edema Furosemide tablets are indicated in adults and pediatric patients for the treatment of edema associated with congestive heart failure, cirrhosis of the liver, and renal disease, including the nephrotic syndrome. Furosemide Tablets are particularly useful when an agent with greater diuretic potential is desired. Hypertension Oral furosemide may be used in adults for the treatment of hypertension alone or in combination with other antihypertensive agents. Hypertensive patients who cannot be adequately controlled with thiazides will probably also not be adequately controlled with furosemide alone.
Excerpt only. Read the full label for complete information.
About NDC 71335-2319
- What is NDC 71335-2319?
- 71335-2319 is the product NDC for Furosemide, Furosemide 20 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 10 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Furosemide.
- What is the active ingredient?
- Furosemide.
- Who is the labeler?
- Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Furosemide?
- 204 other product NDCs are listed under this name. See all Furosemide NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Furosemide products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Furosemide | Furosemide 10 mg/mL | InjectionIntramuscular, Intravenous | Civica, Inc. | 72572-275 | 72572-0275-10 |
| Furosemide | Furosemide 20 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4679 | 70518-4679-00 |
| Furosemide | Furosemide 20 mg/1 | TabletOral | Unit Dose Solutions, Inc. | 87441-033 | 87441-0033-01 |
| Furosemide | Furosemide 20 mg/1 | TabletOral | Coupler LLC | 67046-0768 | 67046-0768-03 |
| Furosemide | Furosemide 40 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4609 | 70518-4609-00 |
| Furosemide | Furosemide 40 mg/1 | TabletOral | Coupler LLC | 67046-1663 | 67046-1663-03 |
| Furosemide | Furosemide 20 mg/1 | TabletOral | Marlex Pharmaceuticals, Inc. | 10135-832 | 10135-0832-0110135-0832-1010135-0832-90 |
| Furosemide | Furosemide 40 mg/1 | TabletOral | Marlex Pharmaceuticals, Inc. | 10135-833 | 10135-0833-0110135-0833-1010135-0833-90 |
| Furosemide | Furosemide 80 mg/1 | TabletOral | Marlex Pharmaceuticals, Inc. | 10135-834 | 10135-0834-0110135-0834-0510135-0834-90 |
| Furosemide | Furosemide 20 mg/1 | TabletOral | Granulation Technology, Inc. | 63561-0164 | 63561-0164-0163561-0164-0263561-0164-09 |
Other NDCs under ANDA 216629
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Furosemide | Furosemide 20 mg/1 | TabletOral | A-S Medication Solutions | 50090-6642 |
| Furosemide | Furosemide 40 mg/1 | TabletOral | A-S Medication Solutions | 50090-6646 |
| Furosemide | Furosemide 40 mg/1 | TabletOral | A-S Medication Solutions | 50090-6647 |
| Furosemide | Furosemide 20 mg/1 | TabletOral | A-S Medication Solutions | 50090-6942 |
| Furosemide | Furosemide 40 mg/1 | TabletOral | St. Mary's Medical Park Pharmacy | 60760-858 |
| Furosemide | Furosemide 20 mg/1 | TabletOral | Rising Pharma Holdings, Inc. | 64980-562 |
| Furosemide | Furosemide 40 mg/1 | TabletOral | Rising Pharma Holdings, Inc. | 64980-563 |
| Furosemide | Furosemide 80 mg/1 | TabletOral | Rising Pharma Holdings, Inc. | 64980-564 |
| Furosemide | Furosemide 20 mg/1 | TabletOral | Redpharm Drug | 67296-2136 |
| Furosemide | Furosemide 40 mg/1 | TabletOral | Redpharm Drug | 67296-2139 |
| Furosemide | Furosemide 40 mg/1 | TabletOral | NuCare Pharmaceuticals,Inc. | 68071-3536 |
| Furosemide | Furosemide 20 mg/1 | TabletOral | NuCare Pharmaceuticals, Inc. | 68071-3673 |
| Furosemide | Furosemide 40 mg/1 | TabletOral | Preferred Pharmaceuticals Inc. | 68788-8799 |
| Furosemide | Furosemide 20 mg/1 | TabletOral | Prefferred Pharmaceuticals Inc. | 68788-8870 |
| Furosemide | Furosemide 20 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-3757 |
| Furosemide | Furosemide 40 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-2317 |
| Furosemide | Furosemide 20 mg/1 | TabletOral | Northwind Health Company, LLC | 82868-050 |