CareOne Miconazole 3
- Product NDC
- 41520-222
- 11-digit product format
- 415200222
- Labeler code
- 41520
- Product ID
- 41520-222_4820b043-32bf-4d18-9dcb-b29c9334807c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole nitrate
- Dosage form
- KIT
- Labeler
- American Sales Company
- Application
- ANDA076357
- Marketing category
- ANDA
- Marketing start
- 2016-10-17
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41520-222 | CAREONE MICONAZOLE 3 (MICONAZOLE NITRATE) KIT [AMERICAN SALES COMPANY] | 6 | Legacy NDC | 20240619_5e0d61ff-497b-47db-a13f-0e3eba824f36.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41520-222-00 | 41520022200 | 1 KIT in 1 CARTON (41520-222-00) * 1 APPLICATOR in 1 POUCH > 5 g in 1 APPLICATOR * 1 TUBE in 1 CARTON > 9 g in 1 TUBE | 1 kit | 2016-10-17 | 0000-00-00 | No | No | Current |