Ranolazine
NDC 71205-868, Ranolazine, tablet, film coated, extended release, from Proficient Rx LP.
- Product NDC
- 71205-868
- Status
- Listed
- Labeler
- Proficient Rx LP
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA211829
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71205-868 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- RANOLAZINE1000 mg/1
Pharmacologic classes
Anti-anginal [EPC]; Cytochrome P450 2D6 Inhibitors [MoA]; Cytochrome P450 3A Inhibitors [MoA]; Organic Cation Transporter 2 Inhibitors [MoA]; P-Glycoprotein Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71205-868-00 | 71205086800 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-868-00) |
| 71205-868-30 | 71205086830 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-868-30) |
| 71205-868-55 | 71205086855 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-868-55) |
| 71205-868-60 | 71205086860 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-868-60) |
| 71205-868-72 | 71205086872 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-868-72) |
| 71205-868-78 | 71205086878 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-868-78) |
| 71205-868-90 | 71205086890 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-868-90) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/989e1688-a0b5-4297-bf91-234de2a0b445
Use it
Look up 71205-868 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71205-868 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71205-868. 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.