NDC 70710-1156-01 - Nortriptyline 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
- 70710-1156
- Requested NDC
- 70710-1156-01
- Package NDCs from labels
- 70710-1156-3, 70710-1156-1, 70710-1156-5, 70710-1156-01
- Manufacturer
- Zydus Pharmaceuticals (USA) Inc. | Zydus Lifesciences Global FZE | Zydus Lifesciences Limited
- Effective date
- 2024-03-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Nortriptyline Hydrochloride Capsules, USP Rx only | Zydus Pharmaceuticals (USA) Inc. | Zydus Lifesciences Global FZE | Zydus Lifesciences Limited | 2024-03-27 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70710-1156-1 | Nortriptyline Hydrochloride | 100 in 1 BOTTLE | CAPSULE | 100 | 2 | |
| 70710-1156-3 | Nortriptyline Hydrochloride | 30 in 1 BOTTLE | CAPSULE | 30 | 2 | |
| 70710-1156-5 | Nortriptyline Hydrochloride | 500 in 1 BOTTLE | CAPSULE | 500 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70710-1156 | NORTRIPTYLINE HYDROCHLORIDE CAPSULE [ZYDUS PHARMACEUTICALS (USA) INC.] | 2 | Current NDC, Legacy NDC, 3 package rows | 20240328_dbe85bdc-17a1-4201-bf48-a52e35d69b68.zip |
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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.