Hydroxychloroquine Sulfate
NDC 71335-3079, Hydroxychloroquine Sulfate, tablet, film coated, from Bryant Ranch Prepack.
- Product NDC
- 71335-3079
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA040766
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3079 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- HYDROXYCHLOROQUINE SULFATE200 mg/1
Pharmacologic classes
Antimalarial [EPC]; Antirheumatic Agent [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71335-3079-1 | 71335307901 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-3079-1) |
| 71335-3079-2 | 71335307902 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-3079-2) |
| 71335-3079-3 | 71335307903 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-3079-3) |
| 71335-3079-4 | 71335307904 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-3079-4) |
| 71335-3079-5 | 71335307905 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-3079-5) |
| 71335-3079-6 | 71335307906 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-3079-6) |
| 71335-3079-7 | 71335307907 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-3079-7) |
| 71335-3079-8 | 71335307908 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-3079-8) |
| 71335-3079-9 | 71335307909 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-3079-9) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/37413f6b-fb68-4e0c-8bcc-c5b76e956dfc
Use it
Look up 71335-3079 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3079 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-3079. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.