Minocycline Hydrochloride
- Product NDC
- 0093-2134
- 11-digit product format
- 000932134
- Labeler code
- 0093
- Product ID
- 0093-2134_b88f4b72-9c50-4aca-9593-2b77be65b36e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA065485
- Marketing category
- ANDA
- Marketing start
- 2018-02-20
- Marketing end
- 2021-04-30
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 65 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0093-2134-56 | 00093213456 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-2134-56) | 2018-02-20 | 2021-04-30 | No | No | Current |