Diclofenac Sodium
NDC 70512-784, Diclofenac Sodium, tablet, delayed release, from SOLA Pharmaceuticals, LLC.
- Product NDC
- 70512-784
- Status
- Listed
- Labeler
- SOLA Pharmaceuticals, LLC
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA075185
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70512-784 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DICLOFENAC SODIUM75 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Decreased Prostaglandin Production [PE]; Nonsteroidal Anti-inflammatory Drug [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70512-784-60 | 70512078460 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (70512-784-60) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/b8072af2-9940-4827-9fbd-de46ad8bf929NADAC price for package 70512078460
GET /v1/drugs/nadac/70512078460
Use it
Look up 70512-784 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70512-784 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70512-784. 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.