Ximino
- Product NDC
- 69489-123
- 11-digit product format
- 694890123
- Labeler code
- 69489
- Product ID
- 69489-123_79105e42-cbd0-4b33-8217-0b57b160700f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- minocycline hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Journey Medical Corporation
- Application
- NDA201922
- Marketing category
- NDA
- Marketing start
- 2020-11-08
- Marketing end
- 0000-00-00
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 135 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69489-123-03 | 69489012303 | 3 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (69489-123-03) | 2020-11-08 | 0000-00-00 | Yes | No | Current |
| 69489-123-30 | 69489012330 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (69489-123-30) | 2020-11-08 | 0000-00-00 | No | No | Current |