AMZEEQ
- Product NDC
- 72356-101
- 11-digit product format
- 723560101
- Labeler code
- 72356
- Product ID
- 72356-101_34965f9e-e8c4-43cb-bd51-97149aeabf82
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- Journey Medical Corporation
- Application
- NDA212379
- Marketing category
- NDA
- Marketing start
- 2020-01-02
- Marketing end
- 0000-00-00
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 40 mg/g
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72356-101-03 | 72356010103 | 1 CAN in 1 CARTON (72356-101-03) > 30 g in 1 CAN | 1 can | 2020-01-02 | 0000-00-00 | No | No | Current |
| 72356-101-90 | 72356010190 | 1 CAN in 1 CARTON (72356-101-90) > 7 g in 1 CAN | 1 can | 2020-01-02 | 0000-00-00 | No | No | Current |
| 72356-101-92 | 72356010192 | 1 CAN in 1 CARTON (72356-101-92) > 3 g in 1 CAN | 1 can | 2020-01-02 | 0000-00-00 | No | No | Current |