Docosanol
- Product NDC
- 41163-722
- 11-digit product format
- 411630722
- Labeler code
- 41163
- Product ID
- 41163-722_062845c3-6d6f-4f23-816a-051185f04143
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Docosanol
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- EQUALINE (SuperValu)
- Application
- ANDA208754
- Marketing category
- ANDA
- Marketing start
- 2019-10-30
- 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 |
|---|
| 41163-722-07 | 41163072207 | 1 TUBE in 1 PACKAGE (41163-722-07) > 2 g in 1 TUBE | 1 tube | 2019-10-30 | 0000-00-00 | No | No | Current |