Adapalene and Benzoyl Peroxide
- Product NDC
- 66993-869
- 11-digit product format
- 669930869
- Labeler code
- 66993
- Product ID
- 66993-869_0b7e4a98-52af-4f19-9b13-1a9238d9811b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- adapalene and benzoyl peroxide
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Prasco Laboratories
- Application
- NDA022320
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2017-08-03
- Marketing end
- 0000-00-00
- Substance
- ADAPALENE; BENZOYL PEROXIDE
- Active strength
- 1 mg/g; 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66993-869 | ADAPALENE AND BENZOYL PEROXIDE GEL [PRASCO LABORATORIES] | 3 | Legacy NDC | 20250125_97d11c85-c5e3-43da-8e6c-205f37b4293c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66993-869-48 | 66993086948 | 45 g in 1 BOTTLE, PUMP (66993-869-48) | 45 g | 2017-08-03 | 0000-00-00 | No | No | Current |