Minocycline Hydrochloride
- Product NDC
- 55700-649
- 11-digit product format
- 557000649
- Labeler code
- 55700
- Product ID
- 55700-649_810a392b-973a-4cf7-8b15-4d6ca84c759c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA065062
- Marketing category
- ANDA
- Marketing start
- 2018-07-06
- Marketing end
- 0000-00-00
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 50 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-649-60 | 55700064960 | 60 CAPSULE in 1 BOTTLE (55700-649-60) | 60 capsule | 2018-12-14 | 0000-00-00 | No | No | Current |
| 55700-649-90 | 55700064990 | 90 CAPSULE in 1 BOTTLE (55700-649-90) | 90 capsule | 2018-07-06 | 0000-00-00 | No | No | Current |