Miconazole 7
- Product NDC
- 0472-0730
- 11-digit product format
- 004720730
- Labeler code
- 0472
- Product ID
- 0472-0730_fb1e266e-2272-4ac5-b8df-0a16251556a1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole Nitrate
- Dosage form
- CREAM
- Route
- VAGINAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA074164
- Marketing category
- ANDA
- Marketing start
- 1997-04-01
- Marketing end
- 2022-10-07
- Substance
- MICONAZOLE NITRATE
- Active strength
- 20 mg/g
- Pharmacologic classes
- Azole Antifungal [EPC], Azoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0472-0730-41 | 00472073041 | 1 TUBE, WITH APPLICATOR in 1 CARTON (0472-0730-41) > 45 g in 1 TUBE, WITH APPLICATOR | 1997-04-01 | 2022-06-30 | No | No | Current |
| 0472-0730-63 | 00472073063 | 1 TUBE, WITH APPLICATOR in 1 CARTON (0472-0730-63) > 45 g in 1 TUBE, WITH APPLICATOR | 1997-04-01 | 2022-08-31 | No | No | Current |