Prescription drug · ANDA
Levofloxacin NDC 76420-817
Levofloxacin 750 mg/1 · Tablet, Film coated · Oral · Asclemed USA, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 76420-817-05 | 7642008170576420081705 | 5 TABLET, FILM COATED in 1 BOTTLE (76420-817-05)Marketed from May 13, 2024 | |
| 76420-817-07 | 7642008170776420081707 | 7 TABLET, FILM COATED in 1 BOTTLE (76420-817-07)Marketed from May 13, 2024 | |
| 76420-817-10 | 7642008171076420081710 | 10 TABLET, FILM COATED in 1 BOTTLE (76420-817-10)Marketed from May 13, 2024 | |
| 76420-817-14 | 7642008171476420081714 | 14 TABLET, FILM COATED in 1 BOTTLE (76420-817-14)Marketed from May 13, 2024 | |
| 76420-817-20 | 7642008172076420081720 | 20 TABLET, FILM COATED in 1 BOTTLE (76420-817-20)Marketed from May 13, 2024 | |
| 76420-817-30 | 7642008173076420081730 | 30 TABLET, FILM COATED in 1 BOTTLE (76420-817-30)Marketed from May 13, 2024 | |
| 76420-817-50 | 7642008175076420081750 | 50 TABLET, FILM COATED in 1 BOTTLE (76420-817-50)Marketed from May 13, 2024 | |
| 76420-817-55 | 7642008175576420081755 | 500 TABLET, FILM COATED in 1 BOTTLE (76420-817-55)Marketed from May 13, 2024 | |
| 76420-817-60 | 7642008176076420081760 | 60 TABLET, FILM COATED in 1 BOTTLE (76420-817-60)Marketed from May 13, 2024 | |
| 76420-817-90 | 7642008179076420081790 | 90 TABLET, FILM COATED in 1 BOTTLE (76420-817-90)Marketed from May 13, 2024 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
- Levofloxacin
- Generic name (nonproprietary)
- levofloxacin
- Active ingredients
- Levofloxacin — 750 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Asclemed USA, Inc.NDC labeler code 76420
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 201043
- Marketing start
- Listing expires
- Identifiers
- Product ID 76420-817_184fff28-0fd3-da61-e063-6294a90ac035SPL ID 184fff28-0fd3-da61-e063-6294a90ac035SPL set ID 2e32a8aa-047b-46c6-b67b-d88a9a0a810bRxCUI 199884, 199885, 311296UNII 6GNT3Y5LMF
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
N476420081705followed by a unit qualifier and the quantityPackage 76420-0817-05. 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 . This label includes a boxed warning.
Indications (excerpt from the label)
Levofloxacin tablets are a fluoroquinolone antibacterial indicated in adults (18 years of age and older) with infections caused by designated, susceptible bacteria and in pediatric patients where indicated ( 1 , 12.4 ). Pneumonia: Nosocomial ( 1.1 ) and Community Acquired ( 1.2, 1.3 ) Skin and Skin Structure Infections (SSSI): Complicated ( 1.4 ) and Uncomplicated ( 1.5 ) Chronic bacterial prostatitis ( 1.6 ) Inhalational Anthrax, Post-Exposure in adult and pediatric patients ( 1.7 ) Plague in adult and pediatric patients ( 1.8 ) Urinary Tract Infections (UTI): Complicated ( 1.9 , 1.10 ) and Uncomplicated ( 1.12 ) Acute Pyelonephritis ( 1.11 ) Acute Bacterial Exacerbation of Chronic Bronchit…
Excerpt only. Read the full label for complete information.
About NDC 76420-817
- What is NDC 76420-817?
- 76420-817 is the product NDC for Levofloxacin, Levofloxacin 750 mg/1 tablet, film coated, listed with the FDA by Asclemed USA, Inc.. It has 10 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Levofloxacin.
- What is the active ingredient?
- Levofloxacin.
- Who is the labeler?
- Asclemed USA, Inc., NDC labeler code 76420. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Levofloxacin?
- 120 other product NDCs are listed under this name. See all Levofloxacin NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Levofloxacin products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| levofloxacin | Levofloxacin 500 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-1358 | 67046-1358-03 |
| levofloxacin | Levofloxacin 500 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-4568 | 70518-4568-00 |
| levofloxacin | Levofloxacin 250 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-1078 | 67046-1078-03 |
| levofloxacin | Levofloxacin 750 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc | 68788-8809 | 68788-8809-0168788-8809-0268788-8809-04+1 more |
| levofloxacin | Levofloxacin 500 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc. | 68788-8772 | 68788-8772-0168788-8772-0268788-8772-03+2 more |
| Levofloxacinllevofloxacin | Levofloxacin 750 mg/1 | Tablet, Film coatedOral | Advanced Rx Pharmacy of Tennessee, LLC | 80425-0388 | 80425-0388-0180425-0388-02 |
| Levofloxacin | Levofloxacin 250 mg/50mL | Injection, SolutionIntravenous | Hospira, Inc | 0409-2220 | 00409-2220-24 |
| Levofloxacin | Levofloxacin 500 mg/100mL | Injection, SolutionIntravenous | Hospira, Inc | 0409-3330 | 00409-3330-24 |
| Levofloxacin | Levofloxacin 750 mg/150mL | Injection, SolutionIntravenous | Hospira, Inc | 0409-4444 | 00409-4444-24 |
| Levofloxacin | Levofloxacin 25 mg/mL | SolutionOral | ANI Pharmaceuticals, Inc. | 70954-852 | 70954-0852-1070954-0852-2070954-0852-30 |
Other NDCs under ANDA 201043
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 |
|---|---|---|---|---|
| Levofloxacin | Levofloxacin 500 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 43063-457 |
| Levofloxacin | Levofloxacin 500 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-3712 |
| Levofloxacin | Levofloxacin 750 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 43063-459 |
| Levofloxacin | Levofloxacin 750 mg/1 | Tablet, Film coatedOral | HAWAII REPACK, INC. | 85534-0098 |
| Levofloxacin | Levofloxacin 250 mg/1 | Tablet, Film coatedOral | HAWAII REPACK, INC. | 85534-0096 |
| Levofloxacin | Levofloxacin 500 mg/1 | Tablet, Film coatedOral | HAWAII REPACK, INC. | 85534-0097 |
| Levofloxacin | Levofloxacin 500 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-1226 |
| Levofloxacin | Levofloxacin 750 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-1228 |
| Levofloxacin | Levofloxacin 500 mg/1 | Tablet, Film coatedOral | Advanced Rx of Tennessee, LLC | 80425-0008 |
| Levofloxacin | Levofloxacin 250 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 71205-058 |
| Levofloxacin | Levofloxacin 750 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 65862-538 |
| Levofloxacin | Levofloxacin 250 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 65862-536 |
| Levofloxacin | Levofloxacin 500 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 65862-537 |
| Levofloxacin | Levofloxacin 250 mg/1 | Tablet, Film coatedOral | Asclemed USA, Inc. | 76420-815 |
| Levofloxacin | Levofloxacin 500 mg/1 | Tablet, Film coatedOral | Asclemed USA, Inc. | 76420-816 |
| Levofloxacin | Levofloxacin 250 mg/1 | Tablet, Film coatedOral | Redpharm Drug | 67296-1104 |
| Levofloxacin | Levofloxacin 500 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 72789-367 |
| Levofloxacin | Levofloxacin 500 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 72789-085 |