minocycline hydrochloride
- Product NDC
- 47781-545
- 11-digit product format
- 477810545
- Labeler code
- 47781
- Product ID
- 47781-545_3ee915be-d5ee-3805-1ad9-092264ecfffd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- minocycline hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Alvogen, Inc.
- Application
- ANDA063067
- Marketing category
- ANDA
- Marketing start
- 2017-10-31
- Marketing end
- 0000-00-00
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 75 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 |
|---|
| 47781-545-01 | 47781054501 | 100 CAPSULE in 1 BOTTLE (47781-545-01) | 100 capsule | 2017-10-31 | 0000-00-00 | No | No | Current |