Minocycline Hydrochloride
- Product NDC
- 50090-2339
- 11-digit product format
- 500902339
- Labeler code
- 50090
- Product ID
- 50090-2339_0a0502f4-9e1e-4e61-9d21-14db04dc723b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065062
- Marketing category
- ANDA
- Marketing start
- 2015-04-02
- 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
- 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 |
|---|
| 50090-2339-0 | 50090233900 | 60 CAPSULE in 1 BOTTLE (50090-2339-0) | 60 capsule | 2016-04-04 | 0000-00-00 | No | No | Current |
| 50090-2339-2 | 50090233902 | 20 CAPSULE in 1 BOTTLE (50090-2339-2) | 20 capsule | 2016-04-04 | 0000-00-00 | No | No | Current |
| 50090-2339-3 | 50090233903 | 30 CAPSULE in 1 BOTTLE (50090-2339-3) | 30 capsule | 2016-04-04 | 0000-00-00 | No | No | Current |
| 50090-2339-4 | 50090233904 | 90 CAPSULE in 1 BOTTLE (50090-2339-4) | 90 capsule | 2016-04-04 | 0000-00-00 | No | No | Current |