TIOCONAZOLE
- Product NDC
- 63094-0426
- 11-digit product format
- 630940426
- Labeler code
- 63094
- Product ID
- 63094-0426_11ddf219-8537-4a8f-b267-ef965159885e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TIOCONAZOLE
- Dosage form
- OINTMENT
- Route
- VAGINAL
- Labeler
- DPT Laboratories, Ltd.
- Application
- ANDA075915
- Marketing category
- ANDA
- Marketing start
- 2007-08-22
- Marketing end
- 0000-00-00
- Substance
- TIOCONAZOLE
- Active strength
- 65 mg/g
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63094-0426-1 | TIOCONAZOLEOintment 6.5% | 5 g in 1 APPLICATOR | OINTMENT | 5 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63094-0426 | TIOCONAZOLE OINTMENT 6.5% (TIOCONAZOLE) OINTMENT [DPT LABORATORIES, LTD. ] | 1 | Legacy NDC, 1 package rows | 20090901_11ddf219-8537-4a8f-b267-ef965159885e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 63094-0426-1 | 63094042601 | 5 g in 1 APPLICATOR | 5 g | Historical |