Diclofenac Sodium
- Product NDC
- 72162-1086
- 11-digit product format
- 721621086
- Labeler code
- 72162
- Product ID
- 72162-1086_b48907d5-f288-41f3-b160-ed26c05290aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076201
- Marketing category
- ANDA
- Marketing start
- 2002-11-06
- Substance
- DICLOFENAC SODIUM
- Active strength
- 100 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| QTG126297Q | DICLOFENAC SODIUM | 15307-79-6 | DICLOFENAC SODIUM |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1086-8 | 72162108608 | 21 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72162-1086-8) | 2023-05-08 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Diclofenac Sodium | Bryant Ranch Prepack | 2023-05-08 | HUMAN PRESCRIPTION DRUG LABEL | 100 |