Miconazole Nitrate
- Product NDC
- 68016-673
- 11-digit product format
- 680160673
- Labeler code
- 68016
- Product ID
- 68016-673_c78df313-72b6-010a-e053-2995a90ac28d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazorb Antifungal Powder Talc Free
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Chain Drug Consortium, LLC
- Application
- part333C
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-10-22
- Marketing end
- 0000-00-00
- Substance
- MICONAZOLE NITRATE
- Active strength
- 1 g/71g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 68016-673 | D | Discontinued by firm | 2026-10-12 | ||
| excluded package | package | 68016-673 | 68016-673-25 | D | Discontinued by firm | 2026-10-12 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 68016-673-25 | 68016067325 | 71 g in 1 BOTTLE, PLASTIC (68016-673-25) | 71 g | 2017-10-22 | 0000-00-00 | No | No | Current |