Miconazole Nitrate
- Product NDC
- 70518-2338
- 11-digit product format
- 705182338
- Labeler code
- 70518
- Product ID
- 70518-2338_e3a16c44-85d8-d5d8-e053-2a95a90a1aa2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole Nitrate
- Dosage form
- CREAM
- Route
- VAGINAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA074444
- Marketing category
- ANDA
- Marketing start
- 2019-10-02
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2338-0 | 70518233800 | 1 TUBE, WITH APPLICATOR in 1 CARTON (70518-2338-0) > 45 g in 1 TUBE, WITH APPLICATOR | 2019-10-02 | 0000-00-00 | No | No | Current |