Diclofenac Sodium
- Product NDC
- 70518-0572
- 11-digit product format
- 705180572
- Labeler code
- 70518
- Product ID
- 70518-0572_beee7d04-ae12-df3b-e053-2a95a90a17f9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Diclofenac Sodium
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202027
- Marketing category
- ANDA
- Marketing start
- 2017-06-12
- Marketing end
- 0000-00-00
- Substance
- DICLOFENAC SODIUM
- Active strength
- 16 mg/mL
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0572-0 | 70518057200 | 1 BOTTLE in 1 CARTON (70518-0572-0) > 150 mL in 1 BOTTLE | 1 bottle | 2017-06-12 | 0000-00-00 | No | No | Current |