miconazole 1
- Product NDC
- 37808-737
- 11-digit product format
- 378080737
- Labeler code
- 37808
- Product ID
- 37808-737_31dd9603-fd6f-4454-92bf-8127af45a5db
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole nitrate
- Dosage form
- KIT
- Labeler
- H E B
- Application
- ANDA079114
- Marketing category
- ANDA
- Marketing start
- 2010-06-07
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record