TERCONAZOLE
- Product NDC
- 50090-2341
- 11-digit product format
- 500902341
- Labeler code
- 50090
- Product ID
- 50090-2341_6d3b1e57-0411-407d-bbd1-14d59cefe9f0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TERCONAZOLE
- Dosage form
- CREAM
- Route
- VAGINAL
- Labeler
- A-S Medication Solutions
- Application
- NDA019579
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2004-04-01
- Marketing end
- 0000-00-00
- Substance
- TERCONAZOLE
- Active strength
- 4 mg/g
- Pharmacologic classes
- Azole Antifungal [EPC],Azoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2341-0 | TERCONAZOLE | 1 in 1 CARTON | CREAM | 1 | | 7 |
| 50090-2341-0 | TERCONAZOLE | 45 g in 1 TUBE, WITH APPLICATOR | CREAM | 45 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2341 | TERCONAZOLE CREAM [A-S MEDICATION SOLUTIONS] | 7 | Legacy NDC, 2 package rows | 20180115_91c8519c-314e-4b30-95a5-aefa3b0338d9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-2341-0 | 50090234100 | 1 in 1 CARTON | Historical |