Minocycline Hydrochloride
- Product NDC
- 42291-620
- 11-digit product format
- 422910620
- Labeler code
- 42291
- Product ID
- 42291-620_d57e4d28-4671-9978-e053-2995a90acd91
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA065062
- Marketing category
- ANDA
- Marketing start
- 2011-07-26
- Marketing end
- 0000-00-00
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 42291-620-05 | 42291062005 | 50 CAPSULE in 1 BOTTLE (42291-620-05) | 50 capsule | 2011-07-26 | 0000-00-00 | No | No | Current |
| 42291-620-50 | 42291062050 | 500 CAPSULE in 1 BOTTLE (42291-620-50) | 500 capsule | 2011-07-26 | 0000-00-00 | No | No | Current |