Miconazole 7
- Product NDC
- 68788-7519
- 11-digit product format
- 687887519
- Labeler code
- 68788
- Product ID
- 68788-7519_2c5ca4a9-cbda-4980-b25f-e74be85b64b8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole Nitrate
- Dosage form
- CREAM
- Route
- VAGINAL
- Labeler
- Preferred Pharmaceuticals, Inc..
- Application
- ANDA074164
- Marketing category
- ANDA
- Marketing start
- 1997-04-01
- 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 |
|---|
| 68788-7519-4 | 68788751904 | 1 TUBE, WITH APPLICATOR in 1 CARTON (68788-7519-4) > 45 g in 1 TUBE, WITH APPLICATOR | 2019-10-28 | 0000-00-00 | No | No | Current |