Prescription drug · ANDA
Zinc Sulfate (Zinc sulfate injection) NDC 60505-6261
Zinc sulfate, Unspecified form 1 mg/mL · Injection · Intravenous · Apotex Corp
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 60505-6261-5 | 6050562610560505626105 | 25 VIAL in 1 CARTON (60505-6261-5) / 10 mL in 1 VIAL (60505-6261-0)Marketed from Jan 15, 2025 |
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)
- Zinc Sulfate
- Generic name (nonproprietary)
- zinc sulfate injection
- Active ingredients
- Zinc sulfate, Unspecified form — 1 mg/mL
- Dosage form
- Injection
- Route
- Intravenous
- Labeler
- Apotex CorpNDC labeler code 60505
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 218059
- Marketing start
- Listing expires
- Other FDA classes
- Decreased Copper Ion Absorption (Physiologic effect)
- Identifiers
- Product ID 60505-6261_5896cfbb-5571-509f-40d9-da61c8263869SPL ID 5896cfbb-5571-509f-40d9-da61c8263869
- Pharmacologic class
- Copper Absorption Inhibitor
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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.
- Administration
Drug administration (CPT 96360–96549)
When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.
- NDC on a medical claim
N460505626105followed by a unit qualifier and the quantityPackage 60505-6261-05. 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
The FDA listing for this product does not reference a label (SPL) set.
About NDC 60505-6261
- What is NDC 60505-6261?
- 60505-6261 is the product NDC for Zinc Sulfate (zinc sulfate injection), Zinc sulfate, Unspecified form 1 mg/mL injection, listed with the FDA by Apotex Corp. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Zinc Sulfate (Zinc Sulfate Injection).
- What is the active ingredient?
- Zinc sulfate, Unspecified form.
- Who is the labeler?
- Apotex Corp, NDC labeler code 60505. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Zinc Sulfate?
- 24 other product NDCs are listed under this name. See all Zinc Sulfate NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Zinc Sulfate products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Zinc Sulfate | Zinc sulfate 1 mg/mL | Injection, SolutionIntravenous | Camber Pharmaceuticals, Inc. | 31722-453 | 31722-0453-31 |
| Zinc Sulfate | Zinc sulfate 3 mg/mL | Injection, SolutionIntravenous | Camber Pharmaceuticals, Inc. | 31722-454 | 31722-0454-31 |
| Zinc Sulfate | Zinc sulfate 5 mg/mL | Injection, SolutionIntravenous | Camber Pharmaceuticals, Inc. | 31722-455 | 31722-0455-31 |
| Zinc Sulfatezinc sulfate injection | Zinc sulfate, Unspecified form 5 mg/mL | InjectionIntravenous | Apotex Corp | 60505-6260 | 60505-6260-05 |
| Zinc sulfate | Zinc sulfate 5 mg/mL | SolutionIntravenous | Somerset Therapeutics, LLC | 70069-691 | 70069-0691-25 |
| Zinc sulfate | Zinc sulfate 3 mg/mL | SolutionIntravenous | Somerset Therapeutics, LLC | 70069-692 | 70069-0692-25 |
| zinc sulfatezinc sulfate injection, | Zinc sulfate 1 mg/mL | SolutionIntravenous | Zydus Pharmaceuticals USA Inc. | 70710-1876 | 70710-1876-07 |
| zinc sulfatezinc sulfate injection, | Zinc sulfate 3 mg/mL | SolutionIntravenous | Zydus Pharmaceuticals USA Inc. | 70710-1877 | 70710-1877-07 |
| zinc sulfatezinc sulfate injection, | Zinc sulfate 5 mg/mL | SolutionIntravenous | Zydus Pharmaceuticals USA Inc. | 70710-1878 | 70710-1878-07 |
| zinc sulfate | Zinc sulfate 1 mg/mL | Injection, SolutionIntravenous | Zydus Lifesciences Limited | 70771-1848 | 70771-1848-07 |
Other NDCs under ANDA 218059
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 |
|---|---|---|---|---|
| Zinc Sulfatezinc sulfate injection | Zinc sulfate, Unspecified form 5 mg/mL | InjectionIntravenous | Apotex Corp | 60505-6260 |