Prescription drug · ANDA
mupirocin NDC 70518-1808
Mupirocin 20 mg/g · Ointment · Topical · REMEDYREPACK INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70518-1808-0 | 7051818080070518180800 | 1 TUBE in 1 CARTON (70518-1808-0) / 22 g in 1 TUBEMarketed from Jan 21, 2019 |
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)
- mupirocin
- Generic name (nonproprietary)
- mupirocin
- Active ingredients
- Mupirocin — 20 mg/g
- Dosage form
- Ointment
- Route
- Topical
- Labeler
- REMEDYREPACK INC.NDC labeler code 70518
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 065123
- Marketing start
- Listing expires
- Other FDA classes
- RNA Synthetase Inhibitors (Mechanism)
- Identifiers
- Product ID 70518-1808_49760a72-901f-99dd-e063-6394a90a5cf9SPL ID 49760a72-901f-99dd-e063-6394a90a5cf9SPL set ID 290b4e51-59b4-429a-987b-715ac817ef2cRxCUI 106346UNII D0GX863OA5
- Pharmacologic class
- RNA Synthetase Inhibitor Antibacterial
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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N470518180800followed by a unit qualifier and the quantityPackage 70518-1808-00. 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)
Mupirocin Ointment USP, 2% is indicated for the topical treatment of impetigo due to susceptible isolates of Staphylococcus aureus (S. aureus) and Streptococcus pyogenes (S. pyogenes) . Mupirocin Ointment USP, 2% is an RNA synthetase inhibitor antibacterial indicated for the topical treatment of impetigo due to susceptible isolates of Staphylococcus aureus and Streptococcus pyogenes. ( 1 )
Excerpt only. Read the full label for complete information.
About NDC 70518-1808
- What is NDC 70518-1808?
- 70518-1808 is the product NDC for mupirocin, Mupirocin 20 mg/g ointment, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- mupirocin.
- What is the active ingredient?
- Mupirocin.
- Who is the labeler?
- REMEDYREPACK INC., NDC labeler code 70518. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for mupirocin?
- 42 other product NDCs are listed under this name. See all mupirocin NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other mupirocin products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Mupirocin | Mupirocin calcium 20 mg/g | CreamTopical | Zydus Lifesciences Limited | 70771-1981 | 70771-1981-0170771-1981-02 |
| Mupirocin | Mupirocin calcium 20 mg/g | CreamTopical | Viona Pharmaceuticals Inc | 72578-130 | 72578-0130-0172578-0130-06 |
| Mupirocin | Mupirocin 20 mg/g | OintmentTopical | PAI Holdings, LLC dba PAI Pharma | 0121-1076 | 00121-1076-50 |
| Mupirocinmupirocin ointment | Mupirocin 20 mg/g | OintmentTopical | Kesin Pharma Corporation | 81033-032 | 81033-0032-5081033-0032-99 |
| Mupirocin | Mupirocin 20 mg/g | OintmentTopical | Encube Ethicals, Inc. | 21922-073 | 21922-0073-0421922-0073-0521922-0073-25 |
| Mupirocin | Mupirocin 20 mg/g | OintmentTopical | Redpharm Drug | 67296-2211 | 67296-2211-01 |
| Mupirocin | Mupirocin calcium 20 mg/g | CreamTopical | Alembic Pharmaceuticals Limited | 46708-624 | 46708-0624-1546708-0624-30 |
| mupirocin | Mupirocin 20 mg/g | OintmentTopical | St. Mary's Medical Park Pharmacy | 60760-960 | 60760-0960-22 |
| mupirocin | Mupirocin 20 mg/g | OintmentTopical | Preferred Pharmaceuticals Inc. | 68788-8642 | 68788-8642-02 |
| Mupirocin | Mupirocin 20 mg/g | OintmentTopical | Preferred Pharmaceuticals Inc. | 68788-8534 | 68788-8534-02 |
Other NDCs under ANDA 065123
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 |
|---|---|---|---|---|
| mupirocin | Mupirocin 20 mg/g | OintmentTopical | ATLANTIC BIOLOGICALS CORP. | 17856-0112 |
| mupirocin | Mupirocin 20 mg/g | OintmentTopical | Padagis Israel Pharmaceuticals Ltd | 45802-112 |
| mupirocin | Mupirocin 20 mg/g | OintmentTopical | A-S Medication Solutions | 50090-1587 |
| mupirocin | Mupirocin 20 mg/g | OintmentTopical | St. Mary's Medical Park Pharmacy | 60760-960 |
| mupirocin | Mupirocin 20 mg/g | OintmentTopical | Proficient Rx LP | 63187-261 |
| mupirocin | Mupirocin 20 mg/g | OintmentTopical | Bryant Ranch Prepack | 63629-8687 |
| mupirocin | Mupirocin 20 mg/g | OintmentTopical | NuCare Pharmaceuticals,Inc. | 68071-4789 |
| mupirocin | Mupirocin 20 mg/g | OintmentTopical | Preferred Pharmaceuticals Inc. | 68788-8642 |
| mupirocin | Mupirocin 20 mg/g | OintmentTopical | Bryant Ranch Prepack | 71335-2829 |
| mupirocin | Mupirocin 20 mg/g | OintmentTopical | Bryant Ranch Prepack | 72162-2270 |
| mupirocin | Mupirocin 20 mg/g | OintmentTopical | Asclemed USA, Inc. | 76420-128 |
| Mupirocinmupirocin ointment | Mupirocin 20 mg/g | OintmentTopical | Kesin Pharma Corporation | 81033-032 |
| mupirocin | Mupirocin 20 mg/g | OintmentTopical | HAWAII REPACK, INC. | 85534-0038 |