NDC 51672-2080-01 - Terbinafine Hydrochloride
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 51672-2080
- Requested NDC
- 51672-2080-01
- Package NDCs from labels
- 51672-2080-1, 51672-2080-2, 51672-2080-8, 51672-2080-9, 51672-2080-6, 51672-2080-3, 51672-2080-4, 51672-2080-01
- Manufacturer
- Preferred Pharmaceuticals, Inc
- Effective date
- 2026-10-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Terbinafine Hydrochloride - Preferred Pharmaceuticals, Inc | Preferred Pharmaceuticals, Inc | 2026-10-09 | HUMAN OTC DRUG LABEL |
| Terbinafine Hydrochloride - A-S Medication Solutions | A-S Medication Solutions | 2026-09-11 | HUMAN OTC DRUG LABEL |
| Terbinafine Hydrochloride Cream 1% Antifungal Cream | Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | 2026-02-20 | HUMAN OTC DRUG LABEL |
| Terbinafine Hydrochloride - A-S Medication Solutions | A-S Medication Solutions | 2023-12-09 | HUMAN OTC DRUG LABEL |
| Terbinafine Hydrochloride - Proficient Rx LP | Proficient Rx LP | 2022-07-01 | HUMAN OTC DRUG LABEL |
| Terbinafine Hydrochloride Cream 1% Antifungal Cream | REMEDYREPACK INC. | 2021-03-31 | HUMAN OTC DRUG LABEL |
| Terbinafine Hydrochloride Cream 1% Antifungal Cream | Physicians Total Care, Inc. | 2014-02-24 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-2080-1 | Terbinafine Hydrochloride | 15 g in 1 TUBE | CREAM | 15 | 6 | |
| 51672-2080-1 | Terbinafine Hydrochloride | 1 in 1 CARTON | CREAM | 1 | 6 | |
| 51672-2080-2 | Terbinafine Hydrochloride | 30 g in 1 TUBE | CREAM | 30 | 6 | |
| 51672-2080-2 | Terbinafine Hydrochloride | 1 in 1 CARTON | CREAM | 1 | 6 | |
| 51672-2080-3 | Terbinafine Hydrochloride | 60 g in 1 TUBE | CREAM | 60 | 6 | |
| 51672-2080-3 | Terbinafine Hydrochloride | 1 in 1 CARTON | CREAM | 1 | 6 | |
| 51672-2080-4 | Terbinafine Hydrochloride | 1 in 1 CARTON | CREAM | 1 | 6 | |
| 51672-2080-4 | Terbinafine Hydrochloride | 15 g in 1 TUBE | CREAM | 15 | 6 | |
| 51672-2080-6 | Terbinafine Hydrochloride | 1 in 1 CARTON | CREAM | 1 | 6 | |
| 51672-2080-6 | Terbinafine Hydrochloride | 45 g in 1 TUBE | CREAM | 45 | 6 | |
| 51672-2080-8 | Terbinafine Hydrochloride | 1 in 1 CARTON | CREAM | 1 | 6 | |
| 51672-2080-8 | Terbinafine Hydrochloride | 12 g in 1 TUBE | CREAM | 12 | 6 | |
| 51672-2080-9 | Terbinafine Hydrochloride | 1 in 1 CARTON | CREAM | 1 | 6 | |
| 51672-2080-9 | Terbinafine Hydrochloride | 24 g in 1 TUBE | CREAM | 24 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-2080 | TERBINAFINE HYDROCHLORIDE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] | 3 | Current NDC, Legacy NDC, 14 package rows | 20210304_92b31fc4-0f02-4857-b11f-49b9f942ee84.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-2080-1 | GM - Gram | 51672-2080 | 5b077eb2-4a3e-4467-b213-af80bebdfea2 | 1 | 2012-07-24 |
| 51672-2080-2 | GM - Gram | 51672-2080 | b99b56d3-5b68-429b-b864-d7cef0ee2970 | 1 | 2012-07-24 |
| 51672-2080-8 | GM - Gram | 51672-2080 | 250969be-c2ab-423f-9beb-f2c9d68abc05 | 1 | 2012-07-24 |
| 51672-2080-9 | GM - Gram | 51672-2080 | b03e439e-fc3f-496d-b719-b958636880ea | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Sterile Water | WATER | Baxter Healthcare Corporation | ef3e79c5-3f58-4b36-a296-64b7d9a651c1 | 2017-10-17 | Warnings, Adverse reactions | 059QF0KO0R |
| Eye Wash | WATER | CVS Pharmacy | 049cee29-7ec2-4d5b-8308-f522acde43a7 | 2017-03-29 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
| a56cf9f2-99f5-42df-a203-f8245c428ae5 | ba1f253f-021b-4857-b015-a72aa9df2d83 | 2014-02-24 | Warnings | a56cf9f2-99f5-42df-a203-f8245c428ae5 ba1f253f-021b-4857-b015-a72aa9df2d83 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.