AZELOMAX FORTE
- Product NDC
- 73237-002
- 11-digit product format
- 732370002
- Labeler code
- 73237
- Product ID
- 73237-002_f1e96883-af8d-3cb9-e053-2995a90abee2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil 5%
- Dosage form
- SOLUTION/ DROPS
- Route
- TOPICAL
- Labeler
- TRILOGIC LTD
- Application
- ANDA076239
- Marketing category
- ANDA
- Marketing start
- 2019-07-10
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 5 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 |
|---|
| 73237-002-01 | AZELOMAX FORTE | 1 in 1 BOX | SOLUTION/ DROPS | 1 | | 2 |
| 73237-002-01 | AZELOMAX FORTE | 60 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73237-002 | AZELOMAX FORTE (MINOXIDIL 5%) SOLUTION/ DROPS [TRILOGIC LTD] | 2 | Legacy NDC, 2 package rows | 20230111_8d596085-ec46-1cfe-e053-2995a90a1684.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 |
|---|
| 73237-002-01 | 73237000201 | 1 BOTTLE, DROPPER in 1 BOX (73237-002-01) > 60 mL in 1 BOTTLE, DROPPER | 2019-07-10 | 0000-00-00 | No | No | Current |