Diclofenac Sodium Delayed Release
NDC 51655-176, Diclofenac Sodium, tablet, delayed release, from Northwind Health Company, LLC.
- Product NDC
- 51655-176
- Status
- Listed
- Labeler
- Northwind Health Company, 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/51655-176 \ -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 |
|---|---|---|
| 51655-176-26 | 51655017626 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-176-26) |
| 51655-176-52 | 51655017652 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-176-52) |
| 51655-176-84 | 51655017684 | 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-176-84) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/c16e7e43-3869-9fef-e053-2995a90a1fdb
Use it
Look up 51655-176 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51655-176 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51655-176. 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.