Minocycline
- Product NDC
- 57664-856
- 11-digit product format
- 576640856
- Labeler code
- 57664
- Product ID
- 57664-856_c280d53e-9455-4942-9baa-b79e14adb10a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- ANDA090217
- Marketing category
- ANDA
- Marketing start
- 2016-01-29
- 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
- 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 |
|---|
| 57664-856-13 | 57664085613 | 500 TABLET, FILM COATED in 1 BOTTLE (57664-856-13) | 2016-01-29 | 0000-00-00 | No | No | Current |
| 57664-856-18 | 57664085618 | 1000 TABLET, FILM COATED in 1 BOTTLE (57664-856-18) | 2016-01-29 | 0000-00-00 | No | No | Current |
| 57664-856-85 | 57664085685 | 50 TABLET, FILM COATED in 1 BOTTLE (57664-856-85) | 2016-01-29 | 0000-00-00 | No | No | Current |
| 57664-856-88 | 57664085688 | 100 TABLET, FILM COATED in 1 BOTTLE (57664-856-88) | 2016-01-29 | 0000-00-00 | No | No | Current |