Miconazole 7
- Product NDC
- 61269-736
- 11-digit product format
- 612690736
- Labeler code
- 61269
- Product ID
- 61269-736_081fb777-9c72-4165-a11e-91cd6dd04000
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole Nitrate
- Dosage form
- SUPPOSITORY
- Route
- VAGINAL
- Labeler
- H2-Pharma, LLC
- Application
- ANDA073507
- Marketing category
- ANDA
- Marketing start
- 2021-05-24
- Marketing end
- 0000-00-00
- Substance
- MICONAZOLE NITRATE
- Active strength
- 100 mg/1
- 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 |
|---|
| 61269-736 | MICONAZOLE 7 (MICONAZOLE NITRATE) SUPPOSITORY [H2-PHARMA, LLC] | 3 | Legacy NDC | 20250413_a003ad26-271f-46af-8b9a-8b7fb80b93ff.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61269-736-07 | 61269073607 | 7 SUPPOSITORY in 1 BOX (61269-736-07) | 7 suppository | 2021-05-24 | 0000-00-00 | No | No | Current |