Adapalene
- Product NDC
- 0781-7142
- 11-digit product format
- 007817142
- Labeler code
- 0781
- Product ID
- 0781-7142_9feed925-532f-4ebd-bf90-c9519ff63f73
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Adapalene
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Sandoz Inc.
- Application
- ANDA200298
- Marketing category
- ANDA
- Marketing start
- 2014-04-28
- Marketing end
- 0000-00-00
- Substance
- ADAPALENE
- Active strength
- 3 mg/g
- Pharmacologic classes
- Retinoid [EPC],Retinoids [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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-7142-19 | 00781714219 | 1 TUBE in 1 CARTON (0781-7142-19) > 45 g in 1 TUBE | 1 tube | 2014-04-28 | 0000-00-00 | No | No | Current |
| 0781-7142-70 | 00781714270 | 1 BOTTLE, PUMP in 1 BOTTLE, PUMP (0781-7142-70) > 45 g in 1 BOTTLE, PUMP | | 2014-04-28 | 0000-00-00 | No | No | Current |