Solodyn
- Product NDC
- 99207-465
- 11-digit product format
- 992070465
- Labeler code
- 99207
- Product ID
- 99207-465_a594be33-33ce-4304-a6fe-65a4eeda3f19
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- minocycline hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bausch Health US LLC
- Application
- NDA050808
- Marketing category
- NDA
- Marketing start
- 2010-09-27
- Marketing end
- 0000-00-00
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 55 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- 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 |
|---|
| 99207-465-02 | 99207046502 | 10 BOTTLE in 1 CARTON (99207-465-02) > 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE | 10 bottle | 2010-09-27 | 0000-00-00 | No | No | Current |
| 99207-465-30 | 99207046530 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (99207-465-30) | | 2010-09-27 | 0000-00-00 | No | No | Current |