NDC 68084-856-11 - Venlafaxine
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
- 68084-856
- Requested NDC
- 68084-856-11
- Package NDCs from labels
- 68084-856-11, 68084-856-01
- Manufacturer
- American Health Packaging
- Effective date
- 2024-08-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Venlafaxine - American Health Packaging | American Health Packaging | 2024-08-09 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68084-856-01 | Venlafaxine | 100 in 1 BOX, UNIT-DOSE | TABLET | 100 | 9 | |
| 68084-856-11 | Venlafaxine | 1 in 1 BLISTER PACK | TABLET | 1 | 9 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 68084-856-01 | EA - Each | 68084-856 | 028d920e-a47f-47d4-b6f4-602d38f642e8 | 1 | 2015-04-03 |
| 68084-856-11 | EA - Each | 68084-856 | 8739fd6f-1a93-4702-9c81-7eed0445a7a1 | 1 | 2015-04-03 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| VENLAFAXINE HYDROCHLORIDE | ACTIVE INGREDIENT | 7D7RX5A8MO | VENLAFAXINE TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| VENLAFAXINE | ACTIVE MOIETY | GRZ5RCB1QG | VENLAFAXINE TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | VENLAFAXINE TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | VENLAFAXINE TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | VENLAFAXINE TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | VENLAFAXINE TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | VENLAFAXINE TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | VENLAFAXINE TABLET [AMERICAN HEALTH PACKAGING] | 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 |
|---|---|---|---|---|---|---|
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | Coupler LLC | 4a007068-89d9-c296-e063-6394a90ad6d0 | 2026-02-04 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| Calamine | FERRIC OXIDE RED | Major Pharmaceuticals | c25be68d-834a-4959-8d47-01ec789406ba | 2026-02-04 | Warnings, Adverse reactions | 1K09F3G675 |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | Bryant Ranch Prepack | 85740bf6-7e88-4a6e-9ec9-3455e3b95e59 | 2026-02-04 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | Bryant Ranch Prepack | ea5914ab-28f3-4cb3-bade-6eaccac214e4 | 2026-02-04 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | Bryant Ranch Prepack | bce7adf8-b4b5-4d7f-bf0d-ae1277ae3a2b | 2026-02-04 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| Aquavit 1 | AQUAVIT 1 | Uriel Pharmacy Inc. | 2354fcfc-05a2-444a-ace4-b3df61413157 | 2026-02-02 | Warnings | 1K09F3G675 |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | QPharma, Inc. | 4992698e-5d5a-6468-e063-6394a90ab404 | 2026-02-01 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| venlafaxine | VENLAFAXINE HYDROCHLORIDE | REMEDYREPACK INC. | b19ec628-4034-4316-ad3d-46c1ee220728 | 2026-01-29 | Boxed warning, Warnings, Adverse reactions | 314277 7D7RX5A8MO |
| venlafaxine | VENLAFAXINE HYDROCHLORIDE | REMEDYREPACK INC. | 806b3e38-3b2a-4aaa-973c-e2d921bb353e | 2026-01-29 | Boxed warning, Warnings, Adverse reactions | 313580 7D7RX5A8MO |
| Calamine | CALAMINE | AMERISOURCE BERGEN | 90d9d908-57ea-4062-ade0-8a4888939c91 | 2026-01-29 | Warnings, Adverse reactions | 1K09F3G675 |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | Preferred Pharmaceuticals Inc. | c4312b7b-7a42-45f1-b6e6-e20ea76020c4 | 2026-01-21 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | Preferred Pharmaceuticals Inc. | e2d5a2d5-5e55-426c-bc8d-d29729eba775 | 2026-01-19 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | AvKARE | 7f224c88-9425-9ef0-01bc-dcf3bdafbd89 | 2026-01-16 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | Zydus Pharmaceuticals USA Inc. | 9fda0f8d-b24e-4581-9dca-7aaaf86e2413 | 2026-01-12 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| First Chakra (Root) 7301 | FIRST CHAKRA (ROOT) | Professional Complementary Health Formulas | 61eb1bbe-6675-4369-b852-18975e6b08c7 | 2026-01-08 | Warnings | 1K09F3G675 |
| Third Chakra (Solar Plexus) 7303 | THIRD CHAKRA (SOLAR PLEXUS) | Professional Complementary Health Formulas | eea89c37-ab87-4cc7-8dfc-e7f42a580dd9 | 2026-01-08 | Warnings | 1K09F3G675 |
| venlafaxine | VENLAFAXINE HYDROCHLORIDE | Northwind Health Company, LLC | f2b5c729-17c8-7ecc-e053-2a95a90a2e53 | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | 313586 7D7RX5A8MO |
| venlafaxine | VENLAFAXINE HYDROCHLORIDE | Northwind Health Company, LLC | fb076577-b9da-c78b-e053-6394a90a107b | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | 313584 7D7RX5A8MO |
| venlafaxine | VENLAFAXINE | Northwind Health Company, LLC | dabfa0f2-0060-f0ee-e053-2a95a90aec9b | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | 313584 7D7RX5A8MO |
| venlafaxine | VENLAFAXINE | Northwind Health Company, LLC | db5f1693-ca64-7a97-e053-2995a90acbff | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | 313580 7D7RX5A8MO |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.