Diclovix
- Product NDC
- 72275-702
- 11-digit product format
- 722750702
- Labeler code
- 72275
- Product ID
- 72275-702_84b45252-fdf5-0ab0-e053-2991aa0ac428
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diclofenac sodium, with camphor, lidocaine, and methyl salicylate patch
- Dosage form
- KIT
- Labeler
- Primary Pharmaceuticals, Inc
- Application
- ANDA202769
- Marketing category
- ANDA
- Marketing start
- 2019-03-17
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72275-702-77 | 72275070277 | 1 KIT in 1 KIT (72275-702-77) * 150 mL in 1 BOTTLE (52565-002-05) * 5 POUCH in 1 BOX (53225-1030-1) > 3 PATCH in 1 POUCH > 8650 mg in 1 PATCH | 1 kit | 2019-03-17 | 0000-00-00 | No | No | Current |