Clindavix
- Product NDC
- 72275-741
- 11-digit product format
- 722750741
- Labeler code
- 72275
- Product ID
- 72275-741_b5a8d8d0-e91e-7a74-e053-2a95a90a4ffc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clindamycin Phosphate, Dimethicone
- Dosage form
- KIT
- Route
- TOPICAL
- Labeler
- Primary Pharmaceuticals, Inc.
- Application
- ANDA064050
- Marketing category
- ANDA
- Marketing start
- 2013-09-17
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 72275-741-77 | 72275074177 | 1 KIT in 1 CARTON (72275-741-77) * 60 mL in 1 BOTTLE, WITH APPLICATOR * 114 g in 1 TUBE | 1 kit | 2020-12-01 | 0000-00-00 | No | No | Current |