Diclofenac Sodium
NDC 71335-0648, Diclofenac Sodium, tablet, film coated, extended release, from Bryant Ranch Prepack.
- Product NDC
- 71335-0648
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA075492
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0648 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DICLOFENAC SODIUM100 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 |
|---|---|---|
| 71335-0648-1 | 71335064801 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-1) |
| 71335-0648-2 | 71335064802 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-2) |
| 71335-0648-3 | 71335064803 | 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-3) |
| 71335-0648-4 | 71335064804 | 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-4) |
| 71335-0648-5 | 71335064805 | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-5) |
| 71335-0648-6 | 71335064806 | 21 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-6) |
| 71335-0648-7 | 71335064807 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-7) |
| 71335-0648-8 | 71335064808 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-8) |
| 71335-0648-9 | 71335064809 | 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0648-9) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/49013aad-475c-4efb-84c6-15a5d4664fbf
Use it
Look up 71335-0648 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0648 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-0648. 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.