NDC 55111-453-79 - 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
- 55111-453
- Requested NDC
- 55111-453-79
- Package NDCs from labels
- 55111-453-30, 55111-453-60, 55111-453-90, 55111-453-01, 55111-453-05, 55111-453-79, 55111-453-78
- Manufacturer
- Dr.Reddy's Laboratories Ltd. | Dr.Reddys Laboratories Limited
- Effective date
- 2018-12-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| VENLAFAXINE - Dr.Reddy's Laboratories Ltd. | Dr.Reddys Laboratories Limited | Dr.Reddy's Laboratories Ltd. | Dr.Reddys Laboratories Limited | 2018-12-06 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55111-453-01 | venlafaxine hydrochloride | 100 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 100 | 8 | |
| 55111-453-05 | venlafaxine hydrochloride | 500 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 500 | 8 | |
| 55111-453-30 | venlafaxine hydrochloride | 30 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 30 | 8 | |
| 55111-453-60 | venlafaxine hydrochloride | 60 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 60 | 8 | |
| 55111-453-78 | venlafaxine hydrochloride | 10 in 1 CARTON | CAPSULE, EXTENDED RELEASE | 10 | 8 | |
| 55111-453-79 | venlafaxine hydrochloride | 10 in 1 BLISTER PACK | CAPSULE, EXTENDED RELEASE | 10 | 8 | |
| 55111-453-90 | venlafaxine hydrochloride | 90 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 90 | 8 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 55111-453-05 | EA - Each | 55111-453 | 8c02cd5e-58a9-479a-af6f-b7c92f5680c3 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
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 |
|---|---|---|---|---|---|---|
| Bombee Honey Daily Glow Shield Sunscreen | HOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE | ABT ASIA Inc. | 56112dff-b091-7a56-e063-6294a90a77d3 | 2026-07-08 | Warnings | 15FIX9V2JP |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | REMEDYREPACK INC. | 4e3053b9-cdec-4f4d-85ae-2e55cf1cc185 | 2026-07-08 | Boxed warning, Warnings, Adverse reactions | 313583 7D7RX5A8MO |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | REMEDYREPACK INC. | 50d3b487-9f65-4e2f-b6eb-9533964f8972 | 2026-07-08 | Boxed warning, Warnings, Adverse reactions | 313581 7D7RX5A8MO |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | REMEDYREPACK INC. | ac9b972d-8b8a-4727-90c2-b208f91272fd | 2026-07-08 | Boxed warning, Warnings, Adverse reactions | 313585 7D7RX5A8MO |
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | DERMIO DERMATOLOGY LLC | 562f5b0d-6a10-305d-e063-6394a90a5980 | 2026-07-08 | Warnings | 15FIX9V2JP |
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | Suzanne's Skin2soul LLC | 562fbaa6-f93a-5ec4-e063-6294a90a9634 | 2026-07-08 | Warnings | 15FIX9V2JP |
| Aussie Betta Tallow Sunscreen SPF50 SPF50 | TITANIUM DIOXIDE AND ZINC OXIDE SUNSCREEN | AUSSIE BETTA HEALTHY CARE PTY LTD | 56007d82-ff5b-6c26-e063-6294a90a09b6 | 2026-07-07 | Warnings | 15FIX9V2JP |
| EELHOE Body Coverage Perfector | TITANIUM DIOXIDE | Shantou Eelhoe Daily Chemical Technology Co., Ltd. | 5610c3b7-456b-3bc1-e063-6394a90a3fa8 | 2026-07-07 | Warnings | 15FIX9V2JP |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | Yaopharma Co., Ltd. | 38fd2c97-cd30-2f7d-e054-00144ff8d46c | 2026-07-07 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| venlafaxine | VENLAFAXINE HYDROCHLORIDE | REMEDYREPACK INC. | 4a82cef5-693e-46e9-90c4-bff753cdce37 | 2026-07-06 | Boxed warning, Warnings, Adverse reactions | 7D7RX5A8MO |
| Premier Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | Emerald Aesthetics LLC | 55f88dd1-346c-22a5-e063-6294a90a711f | 2026-07-06 | Warnings | 15FIX9V2JP |
| Dr. Drop NMN Vital Balance (Drop No.1 Cream 90g) | NMN (NICOTINAMIDE MONONUCLEOTIDE), ECTOIN (ECTOINE) | Reedfresh Co., LTD | 55d703ca-ff9d-0dbc-e063-6294a90ab6b1 | 2026-07-05 | Warnings | C9H2L21V7U |
| OHUI Ultimate Cover CC Cushion Compact 02 Natural Beige | TITANIUM DIOXIDE | LG H&H Co., Ltd. | d307471c-6cc6-ce48-e053-2995a90a3e02 | 2026-07-02 | Warnings | 15FIX9V2JP |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | A-S Medication Solutions | f50029b8-7d05-445a-9d9f-71a1aee6088b | 2026-07-01 | Boxed warning, Warnings, Adverse reactions | 313585 7D7RX5A8MO |
| Evereden Fluid Silk Mineral Sunscreen PRO SPF50 | TITANIUM DIOXIDE, ZINC OXIDE | Eden Brands Inc. | 2cb7773f-9a05-ad02-e063-6294a90af024 | 2026-07-01 | Warnings | 15FIX9V2JP |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | A-S Medication Solutions | 5a990dbd-f280-4caf-b950-4703ee98b230 | 2026-07-01 | Boxed warning, Warnings, Adverse reactions | 313583 7D7RX5A8MO |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | A-S Medication Solutions | d94e5404-f728-4e4b-af99-8a8e4dfae227 | 2026-07-01 | Boxed warning, Warnings, Adverse reactions | 313585 7D7RX5A8MO |
| Venlafaxine Hydrochloride | VENLAFAXINE HYDROCHLORIDE | A-S Medication Solutions | c37a73fa-ceee-4555-a61b-e1e66ad6e97d | 2026-07-01 | Boxed warning, Warnings, Adverse reactions | 313581 7D7RX5A8MO |
| OHUI Ultimate Cover CC Cushion Compact 01 Light Beige | TITANIUM DIOXIDE | LG H&H Co., Ltd. | d2f9c54b-ac4e-5141-e053-2a95a90aa2b8 | 2026-06-30 | Warnings | 15FIX9V2JP |
| Calamine Plus Pramoxine HCl | CALAMINE PLUS SPRAY | Target Corporation | 36602b7a-99c0-f6a4-e063-6294a90a8758 | 2026-06-29 | Warnings | 1K09F3G675 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.