NDC 0536-3701-01 - Tepanil
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
- 0536-3701
- Requested NDC
- 0536-3701-01
- Package NDCs from labels
- 0536-3701-01, 0536-3701-02
- Manufacturer
- Qualitest Products, Inc.
- Effective date
- 2006-07-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Tepanil - Qualitest Products, Inc. | Qualitest Products, Inc. | 2006-07-26 | HUMAN PRESCRIPTION DRUG LABELING |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| diethylpropion hydrochloride | ACTIVE INGREDIENT | 19V2PL39NG | TEPANIL (DIETHYLPROPION HYDROCHLORIDE) TABLET, EXTENDED RELEASE [QUALITEST PRODUCTS, INC.] | 1 | |
| diethylpropion | ACTIVE MOIETY | Q94YYU22B8 | TEPANIL (DIETHYLPROPION HYDROCHLORIDE) TABLET, EXTENDED RELEASE [QUALITEST PRODUCTS, INC.] | 1 | |
| carbomer | INACTIVE INGREDIENT | TEPANIL (DIETHYLPROPION HYDROCHLORIDE) TABLET, EXTENDED RELEASE [QUALITEST PRODUCTS, INC.] | 1 | ||
| mannitol | INACTIVE INGREDIENT | 3OWL53L36A | TEPANIL (DIETHYLPROPION HYDROCHLORIDE) TABLET, EXTENDED RELEASE [QUALITEST PRODUCTS, INC.] | 1 | |
| povidone | INACTIVE INGREDIENT | TEPANIL (DIETHYLPROPION HYDROCHLORIDE) TABLET, EXTENDED RELEASE [QUALITEST PRODUCTS, INC.] | 1 | ||
| tartaric acid | INACTIVE INGREDIENT | W4888I119H | TEPANIL (DIETHYLPROPION HYDROCHLORIDE) TABLET, EXTENDED RELEASE [QUALITEST PRODUCTS, INC.] | 1 | |
| zinc stearate | INACTIVE INGREDIENT | H92E6QA4FV | TEPANIL (DIETHYLPROPION HYDROCHLORIDE) TABLET, EXTENDED RELEASE [QUALITEST PRODUCTS, INC.] | 1 |
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 |
|---|---|---|---|---|---|---|
| 79b15110-e484-4b84-8947-15653746773c | 79b15110-e484-4b84-8947-15653746773c | 2006-07-26 | Warnings, Adverse reactions | 79b15110-e484-4b84-8947-15653746773c 79b15110-e484-4b84-8947-15653746773c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.