Diclofenac Sodium Delayed Release
NDC 71335-0481, Diclofenac Sodium, tablet, delayed release, from Bryant Ranch Prepack.
- Product NDC
- 71335-0481
- 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/71335-0481 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DICLOFENAC SODIUM50 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 |
|---|---|---|
| 71335-0481-1 | 71335048101 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-1) |
| 71335-0481-2 | 71335048102 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-2) |
| 71335-0481-3 | 71335048103 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-3) |
| 71335-0481-4 | 71335048104 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-4) |
| 71335-0481-5 | 71335048105 | 20 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-5) |
| 71335-0481-6 | 71335048106 | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-6) |
| 71335-0481-7 | 71335048107 | 14 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-7) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/ae0add8e-3a8a-4c5d-af3b-907f64211fef
Use it
Look up 71335-0481 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0481 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-0481. 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.