Minocycline Hydrochloride
- Product NDC
- 14789-202
- 11-digit product format
- 147890202
- Labeler code
- 14789
- Product ID
- 14789-202_b9a35842-369f-4743-aad8-cf8d90be745e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Nexus Pharmaceuticals Inc.
- Application
- ANDA214934
- Marketing category
- ANDA
- Marketing start
- 2022-10-01
- 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
- 2023-12-31
- 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 |
|---|
| 14789-202-05 | 14789020205 | 10 VIAL, SINGLE-DOSE in 1 CARTON (14789-202-05) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (14789-202-07) | 2022-10-01 | 0000-00-00 | No | No | Current |