Miconazole 7
- Product NDC
- 70518-3202
- 11-digit product format
- 705183202
- Labeler code
- 70518
- Product ID
- 70518-3202_e39af015-ef0b-7c7b-e053-2a95a90a9816
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole Nitrate
- Dosage form
- CREAM
- Route
- VAGINAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA074164
- Marketing category
- ANDA
- Marketing start
- 2021-08-27
- Marketing end
- 0000-00-00
- Substance
- MICONAZOLE NITRATE
- Active strength
- 20 mg/g
- Pharmacologic classes
- Azole Antifungal [EPC], Azoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| VW4H1CYW1K | MICONAZOLE NITRATE | 22832-87-7 | MICONAZOLE NITRATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3202-0 | 70518320200 | 1 TUBE, WITH APPLICATOR in 1 CARTON (70518-3202-0) > 45 g in 1 TUBE, WITH APPLICATOR | 2021-08-27 | 0000-00-00 | No | No | Current |