Minocycline Hydrochloride
- Product NDC
- 16714-103
- 11-digit product format
- 167140103
- Labeler code
- 16714
- Product ID
- 16714-103_eba34835-21e0-44ef-838f-ab2b94fda592
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NorthStar Rx LLC
- Application
- ANDA202261
- Marketing category
- ANDA
- Marketing start
- 2019-08-21
- Marketing end
- 0000-00-00
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 55 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 |
|---|
| 16714-103-01 | 16714010301 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-103-01) | 2019-08-21 | 0000-00-00 | No | No | Current |