Miconazole 7
- Product NDC
- 70518-2396
- 11-digit product format
- 705182396
- Labeler code
- 70518
- Product ID
- 70518-2396_c8e825e3-37e2-1b18-e053-2995a90a8033
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole Nitrate
- Dosage form
- CREAM
- Route
- VAGINAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA074164
- Marketing category
- ANDA
- Marketing start
- 2019-10-29
- Marketing end
- 0000-00-00
- Substance
- MICONAZOLE NITRATE
- Active strength
- 20 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 70518-2396-0 | 70518239600 | 1 TUBE, WITH APPLICATOR in 1 CARTON (70518-2396-0) > 45 g in 1 TUBE, WITH APPLICATOR | 2019-10-29 | 0000-00-00 | No | No | Current |