Prescription drug · ANDA
Hydroxychloroquine sulfate NDC 57664-761
Hydroxychloroquine sulfate 200 mg/1 · Tablet · Oral · Sun Pharmaceutical Industries, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 57664-761-13 | 5766407611357664076113 | 500 TABLET in 1 BOTTLE (57664-761-13)Marketed from Jun 18, 2018 | |
| 57664-761-88 | 5766407618857664076188 | 100 TABLET in 1 BOTTLE (57664-761-88)Marketed from Jun 18, 2018 |
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)
- Hydroxychloroquine sulfate
- Generic name (nonproprietary)
- hydroxychloroquine sulfate
- Active ingredients
- Hydroxychloroquine sulfate — 200 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Sun Pharmaceutical Industries, Inc.NDC labeler code 57664
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 201691
- Marketing start
- Listing expires
- Identifiers
- Product ID 57664-761_cb7adb60-886b-4415-9b04-b6d37712bbe0SPL ID cb7adb60-886b-4415-9b04-b6d37712bbe0SPL set ID 6e72fe06-7995-3fd7-e053-2a91aa0a54dbRxCUI 979092UNII 8Q2869CNVH
- Pharmacologic class
- Antimalarial; Antirheumatic Agent
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
N457664076113followed by a unit qualifier and the quantityPackage 57664-0761-13. 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)
Hydroxychloroquine sulfate tablets are antimalarial and antirheumatic indicated for the: • Treatment of uncomplicated malaria due to Plasmodium falciparum, Plasmodium malariae, Plasmodium ovale, and Plasmodium vivax in adult and pediatric patients. ( 1.1 ) • Prophylaxis of malaria in geographic areas where chloroquine resistance is not reported in adult and pediatric patients. ( 1.1 ) • Treatment of rheumatoid arthritis in adults. ( 1.2 ) • Treatment of systemic lupus erythematosus in adults. ( 1.3 ) • Treatment of chronic discoid lupus erythematosus in adults. ( 1.4 ) Limitations of Use ( 1.1 ): Hydroxychloroquine sulfate tablets are not recommended for the: • Treatment of complicated malar…
Excerpt only. Read the full label for complete information.
About NDC 57664-761
- What is NDC 57664-761?
- 57664-761 is the product NDC for Hydroxychloroquine sulfate, Hydroxychloroquine sulfate 200 mg/1 tablet, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Hydroxychloroquine sulfate.
- What is the active ingredient?
- Hydroxychloroquine sulfate.
- Who is the labeler?
- Sun Pharmaceutical Industries, Inc., NDC labeler code 57664. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Hydroxychloroquine sulfate?
- 51 other product NDCs are listed under this name. See all Hydroxychloroquine sulfate NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Hydroxychloroquine 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) |
|---|---|---|---|---|---|
| Hydroxychloroquine Sulfate | Hydroxychloroquine sulfate 200 mg/1 | TabletOral | Aphena Pharma Solutions - Tennessee, LLC | 53401-040 | 53401-0040-5353401-0040-6053401-0040-70+1 more |
| Hydroxychloroquine Sulfate | Hydroxychloroquine sulfate 200 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-2813 | 71335-2813-01 |
| Hydroxychloroquine Sulfate | Hydroxychloroquine sulfate 200 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-2814 | 71335-2814-01 |
| Hydroxychloroquine Sulfate | Hydroxychloroquine sulfate 200 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-3113 | 71335-3113-0171335-3113-0271335-3113-03+6 more |
| Hydroxychloroquine Sulfate | Hydroxychloroquine sulfate 200 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-3142 | 71335-3142-0171335-3142-0271335-3142-03+6 more |
| Hydroxychloroquine Sulfate | Hydroxychloroquine sulfate 200 mg/1 | TabletOral | Bryant Ranch Prepack | 72162-2467 | 72162-2467-0172162-2467-05 |
| Hydroxychloroquine Sulfate | Hydroxychloroquine sulfate 200 mg/1 | TabletOral | Creekwood Pharmaceuticals LLC | 82619-131 | 82619-0131-0182619-0131-0282619-0131-03 |
| Hydroxychloroquine Sulfate | Hydroxychloroquine sulfate 200 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 59651-889 | 59651-0889-0159651-0889-05 |
| Hydroxychloroquine Sulfate | Hydroxychloroquine sulfate 200 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-1523 | 67046-1523-03 |
| Hydroxychloroquine Sulfate | Hydroxychloroquine sulfate 200 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-3079 | 71335-3079-0171335-3079-0271335-3079-03+6 more |