minocycline hydrochloride
- Product NDC
- 68682-468
- 11-digit product format
- 686820468
- Labeler code
- 68682
- Product ID
- 68682-468_52b31525-c422-4c07-96b9-7e740c4914ee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- minocycline hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Oceanside Pharmaceuticals
- Application
- NDA050808
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2018-10-10
- Marketing end
- 0000-00-00
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 105 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 68682-468-30 | 68682046830 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-468-30) | 2018-10-10 | 0000-00-00 | No | No | Current |