AXELOFEIN
- Product NDC
- 73237-001
- 11-digit product format
- 732370001
- Labeler code
- 73237
- Product ID
- 73237-001_f1e96716-1fa0-51b5-e053-2a95a90a774d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil 2%
- Dosage form
- SOLUTION/ DROPS
- Route
- TOPICAL
- Labeler
- TRILOGIC, LTD
- Application
- ANDA078176
- Marketing category
- ANDA
- Marketing start
- 2019-07-10
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 2 g/100mL
- Pharmacologic classes
- Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73237-001-01 | AXELOFEIN | 60 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 60 | | 2 |
| 73237-001-01 | AXELOFEIN | 1 in 1 BOX | SOLUTION/ DROPS | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73237-001 | AXELOFEIN (MINOXIDIL 2%) SOLUTION/ DROPS [TRILOGIC, LTD] | 2 | Legacy NDC, 2 package rows | 20230111_8d59713e-7925-1d00-e053-2995a90a4d67.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73237-001-01 | 73237000101 | 1 BOTTLE, DROPPER in 1 BOX (73237-001-01) > 60 mL in 1 BOTTLE, DROPPER | 2019-07-10 | 0000-00-00 | No | No | Current |