NDC 70710-1699-2 - 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
- 70710-1699
- Requested NDC
- 70710-1699-2
- Package NDCs from labels
- 70710-1699-5, 70710-1699-0, 70710-1699-2, 70710-1699-4, 70710-1699-3, 70710-1699-9
- 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 |
| Venlafaxine Hydrochloride - REMEDYREPACK INC. | REMEDYREPACK INC. | 2024-05-07 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70710-1699-0 | Venlafaxine Hydrochloride | 1000 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 1000 | 3 | |
| 70710-1699-2 | Venlafaxine Hydrochloride | 10 in 1 BLISTER PACK | CAPSULE, EXTENDED RELEASE | 10 | 3 | |
| 70710-1699-3 | Venlafaxine Hydrochloride | 30 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 30 | 3 | |
| 70710-1699-4 | Venlafaxine Hydrochloride | 10 in 1 CARTON | CAPSULE, EXTENDED RELEASE | 10 | 3 | |
| 70710-1699-5 | Venlafaxine Hydrochloride | 500 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 500 | 3 | |
| 70710-1699-9 | Venlafaxine Hydrochloride | 90 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 90 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70710-1699 | 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 |
|---|---|---|---|---|---|
| 70710-1699-0 | EA - Each | 70710-1699 | 8f29174b-5928-46b7-87bf-6db9cce308f7 | 1 | 2024-04-05 |
| 70710-1699-9 | EA - Each | 70710-1699 | cea40c4a-925a-4aa8-8a92-9bc90ac71944 | 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 |
|---|---|---|---|---|---|---|
| Anubis Barcelona | FERULIC ACID, VITAMIN C, DMAE | ANUBIS COSMETICS SL | eaf0770c-795d-0232-e053-2a95a90ae0b5 | 2023-09-01 | Warnings | 059QF0KO0R |
| Anubis Barcelona Regul OIl | PEG-40 HYDROGENATED CASTOR OIL, PROPYLENE GLYCOL, ARCTIUM MAJUS ROOT EXTRACT | ANUBIS COSMETICS SL | eb905bd0-c600-b8b2-e053-2995a90ad259 | 2023-09-01 | Warnings | 6DC9Q167V3 059QF0KO0R |
| Anubis Barcelona Regul Oil | PROPYLENE GLYCOL, GLYCERYL STEARATE SE, HUMULUS LUPULUS (HOPS) CONE EXTRACT | ANUBIS COSMETICS SL | eb7c418b-8bee-26a3-e053-2a95a90a4e96 | 2023-09-01 | Warnings | 6DC9Q167V3 059QF0KO0R |
| Anubis Barcelona Total Hydrating | BETAINE, GLYCERIN, POLYSORBATE 20 | ANUBIS COSMETICS SL | eaefe3b9-9064-18b1-e053-2a95a90a5765 | 2023-09-01 | Warnings | 059QF0KO0R |
| Anubis Barcelona New Even | LACTIC ACID, CITRIC ACID, GLYCOLIC ACID | ANUBIS COSMETICS SL | eaeeb6e0-5322-20c4-e053-2995a90a9fd9 | 2023-09-01 | Warnings | 6DC9Q167V3 059QF0KO0R |
| Venlafaxine | VENLAFAXINE | Zydus Pharmaceuticals USA Inc. | db1d16b3-d1a2-4f41-adff-a87c17689aa0 | 2023-09-01 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| Venlafaxine | VENLAFAXINE | BluePoint Laboratories | 172b3d3d-bdae-47bf-8fba-edd6da1a8649 | 2023-08-31 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| Anubis Barcelona Vital Line | HYDROLYZED COLLAGEN | ANUBIS COSMETICS SL | f564bbf0-3b5c-4a81-e053-2a95a90a7ea6 | 2023-08-29 | Warnings | 059QF0KO0R |
| Venlafaxine | VENLAFAXINE | Zydus Pharmaceuticals USA Inc. | 72efad5f-0909-46a5-aa13-ac24fe015fe6 | 2023-08-26 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | Teva Pharmaceuticals USA, Inc. | 37aaa8ac-4e0c-4e04-98b5-19b0d90d857c | 2023-08-25 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| venlafaxine | VENLAFAXINE | Alembic Pharmaceuticals Inc. | 67b323a7-a8c9-410f-bff0-0e515bef41a7 | 2023-08-23 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| Venlafaxine | VENLAFAXINE HYDROCHLORIDE | Aurobindo Pharma Limited | b23637e5-d37f-41b5-ba76-fc053e903bc2 | 2023-08-21 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| venlafaxine | VENLAFAXINE HYDROCHLORIDE | Rising Pharma Holdings, Inc. | 20319949-ccf9-477a-a6e3-53502772deb9 | 2023-08-19 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| Effexor XR | VENLAFAXINE HYDROCHLORIDE | Viatris Specialty LLC | c848a5d8-ba94-4c84-80e3-0bf35fb8e32e | 2023-08-15 | Boxed warning, Warnings, Adverse reactions | 313585 313583 313581 7D7RX5A8MO |
| VENLAFAXINE | VENLAFAXINE | Cadila Pharmaceuticals Limited | 2ed61dcf-42e3-47cf-a607-459eef5fea98 | 2023-08-01 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | A-S Medication Solutions | 52319578-f7cc-4b87-b532-f341854e40b4 | 2023-07-22 | Boxed warning, Warnings, Adverse reactions | 313583 7D7RX5A8MO |
| Household Antigens | ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, ANACARDIUM ORIENTALE, GRAPHITES, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), SULPHUR | BioActive Nutritional | 3382df85-3ec5-4371-830e-4ed345b8f51b | 2023-07-14 | Warnings | 6DC9Q167V3 368GB5141J |
| Pneumotox | TRITICUM AESTIVUM, ALFALFA, ARNICA MONTANA, ASCLEPIAS TUBEROSA, CHAMOMILLA, ECHINACEA (ANGUSTIFOLIA), EUCALYPTUS GLOBULUS, FUCUS VESICULOSUS, HORDEUM VULGARE, IODIUM, NASTURTIUM AQUATICUM, PLANTAGO MAJOR, RAPHANUS SATIVUS, TRIFOLIUM PRATENSE, TRIGONELLA FOENUM-GRAECUM, SYMPHYTUM OFFICINALE, LUNG (SUIS), ORYZA SATIVA, SILICEA, ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, ARSENICUM ALBUM, NATRUM MURIATICUM, NITRICUM ACIDUM, | BioActive Nutritional, Inc. | f8846fb1-92e5-4f8e-b3b3-bc620df90a62 | 2023-07-12 | Warnings | 6DC9Q167V3 368GB5141J |
| Sheer Tint Mineral Sunscreen Broad Spectrum SPF 50 - Light/Medium Shade | SPF 50 SUNSCREEN BROAD SPECTRUM - LIGHT/MEDIUM SHADE | Autumn Harp | fd6807e1-c8c0-b361-e053-6294a90aea0c | 2023-06-05 | Warnings | 15FIX9V2JP |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | Proficient Rx LP | 922388b3-fc1c-46c6-b314-9049bd042df7 | 2023-06-01 | Boxed warning, Warnings, Adverse reactions | 313583 7D7RX5A8MO |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.