Docosanol
- Product NDC
- 41250-932
- 11-digit product format
- 412500932
- Labeler code
- 41250
- Product ID
- 41250-932_8923f39c-9b99-4e31-8c1d-b93991b9d9e9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Docosanol
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- MEIJER, INC.
- Application
- ANDA208754
- Marketing category
- ANDA
- Marketing start
- 2020-04-01
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41250-932-07 | 41250093207 | 1 TUBE in 1 PACKAGE (41250-932-07) > 2 g in 1 TUBE | 1 tube | 2020-04-01 | 0000-00-00 | No | No | Current |