DOCOSANOL
- Product NDC
- 71589-019
- 11-digit product format
- 715890019
- Labeler code
- 71589
- Product ID
- 71589-019_79d7df50-7ce1-4679-b638-224ae611969c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DOCOSANOL
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Aleor Dermaceuticals Limited
- Application
- ANDA215839
- Marketing category
- ANDA
- Marketing start
- 2022-05-03
- Marketing end
- 0000-00-00
- Substance
- DOCOSANOL
- Active strength
- 100 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71589-019-01 | 71589001901 | 1 TUBE in 1 PACKAGE (71589-019-01) > 2 g in 1 TUBE | 1 tube | 2022-05-03 | 0000-00-00 | No | No | Current |
| 71589-019-03 | 71589001903 | 1 BOTTLE, PUMP in 1 PACKAGE (71589-019-03) > 2 g in 1 BOTTLE, PUMP | | 2022-05-03 | 0000-00-00 | No | No | Current |