Diclofenac Sodium Delayed Release
NDC 63629-2012, Diclofenac Sodium, tablet, delayed release, from Bryant Ranch Prepack.
- Product NDC
- 63629-2012
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- 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/63629-2012 \ -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 |
|---|---|---|
| 63629-2012-1 | 63629201201 | 12 BOTTLE, PLASTIC in 1 BOX (63629-2012-1) / 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/bced0ef0-085a-40db-9678-2bc6eb77d456
Use it
Look up 63629-2012 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/63629-2012 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 63629-2012. 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.