NDC 70710-1698-2 - Venlafaxine 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
- 70710-1698
- Requested NDC
- 70710-1698-2
- Package NDCs from labels
- 70710-1698-9, 70710-1698-0, 70710-1698-2, 70710-1698-4, 70710-1698-3, 70710-1698-5
- Manufacturer
- Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited
- Effective date
- 2026-01-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| VENLAFAXINE - Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited | Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited | 2026-01-12 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70710-1698-0 | Venlafaxine Hydrochloride | 1000 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 1000 | 3 | |
| 70710-1698-2 | Venlafaxine Hydrochloride | 10 in 1 BLISTER PACK | CAPSULE, EXTENDED RELEASE | 10 | 3 | |
| 70710-1698-3 | Venlafaxine Hydrochloride | 30 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 30 | 3 | |
| 70710-1698-4 | Venlafaxine Hydrochloride | 10 in 1 CARTON | CAPSULE, EXTENDED RELEASE | 10 | 3 | |
| 70710-1698-5 | Venlafaxine Hydrochloride | 500 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 500 | 3 | |
| 70710-1698-9 | Venlafaxine Hydrochloride | 90 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 90 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70710-1698 | VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [ZYDUS PHARMACEUTICALS USA INC.] | 2 | Current NDC, 6 package rows | 20230905_9fda0f8d-b24e-4581-9dca-7aaaf86e2413.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70710-1698-0 | EA - Each | 70710-1698 | d12d659f-38e7-4ec1-a704-619bc60a02db | 1 | 2024-04-05 |
| 70710-1698-9 | EA - Each | 70710-1698 | 549c8633-83bc-40bf-8752-898b7405a9c3 | 1 | 2024-04-05 |
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 |
|---|---|---|---|---|---|---|
| Meijer Kids Tear Free SPF 50 | TITANIUM DIOXIDE, ZINC OXIDE | Meijer Distribution, Inc. | 7415511e-1ecf-4646-b64b-267fbf7d116b | 2016-06-02 | Warnings | 15FIX9V2JP |
| Meijer Baby Tear Free SPF 50 | TITANIUM DIOXIDE, ZINC OXIDE | Meijer Distributing Inc. | 2434de23-bcc9-4a83-9945-16fc3f2b8c61 | 2016-06-01 | Warnings | 15FIX9V2JP |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
| TOTAL DEFENSE REPAIR BROAD SPECTRUM SPF 34 Sunscreen (Tinted) | OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE AND ZINC OXIDE | Allergan, Inc. | 6a996e03-907f-4e6a-b232-0892b86956b0 | 2015-08-21 | Warnings | 15FIX9V2JP |
| Renewal Firming Day Broad Spectrum SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | BURT'S BEES, INC. | 18ceb5d8-4b76-6a54-e054-00144ff88e88 | 2015-06-18 | Warnings | 15FIX9V2JP |
| TiZO2 | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals, LTD. | 30468afc-9616-4765-b046-12e97a0a7827 | 2010-12-20 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.