Antifungal Foot
- Product NDC
- 41520-080
- 11-digit product format
- 415200080
- Labeler code
- 41520
- Product ID
- 41520-080_23325692-c7be-4e4b-b7ea-09d5fe8578f0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Terbinafine Hydrochloride
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- American Sales Company
- Application
- ANDA077511
- Marketing category
- ANDA
- Marketing start
- 2007-07-02
- Marketing end
- 0000-00-00
- Substance
- TERBINAFINE HYDROCHLORIDE
- Active strength
- 1 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 41520-080-02 | Antifungal Foot | 30 g in 1 TUBE | CREAM | 30 | | 3 |
| 41520-080-02 | Antifungal Foot | 1 in 1 CARTON | CREAM | 1 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41520-080 | ANTIFUNGAL FOOT (TERBINAFINE HYDROCHLORIDE) CREAM [AMERICAN SALES COMPANY] | 3 | Legacy NDC, 2 package rows | 20241012_3da3a963-b5c5-4195-9feb-7dc51a7321c9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41520-080-02 | 41520008002 | 1 TUBE in 1 CARTON (41520-080-02) > 30 g in 1 TUBE | 1 tube | 2007-07-02 | 0000-00-00 | No | No | Current |