Minocycline Hydrochloride
- Product NDC
- 72143-223
- 11-digit product format
- 721430223
- Labeler code
- 72143
- Product ID
- 72143-223_2cddc64f-78ca-4823-8641-93cf457c75a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- minocycline hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- JG Pharma, Inc.
- Application
- NDA201922
- Marketing category
- NDA
- Marketing start
- 2020-04-20
- Marketing end
- 0000-00-00
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 135 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72143-223-30 | 72143022330 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72143-223-30) | 2020-04-20 | 0000-00-00 | No | No | Current |