NDC 70518-3815-01 - Meclizine 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
- 70518-3815
- Requested NDC
- 70518-3815-01
- Package NDCs from labels
- 70518-3815-0, 70518-3815-1, 70518-3815-2, 70518-3815-3, 70518-3815-4, 70518-3815-5, 70518-3815-6, 70518-3815-01
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-09-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Meclizine Hydrochloride - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-09-01 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-3815-0 | Meclizine Hydrochloride | 21 in 1 BOTTLE, PLASTIC | TABLET | 21 | 9 | |
| 70518-3815-1 | Meclizine Hydrochloride | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | 9 | |
| 70518-3815-2 | Meclizine Hydrochloride | 30 in 1 BLISTER PACK | TABLET | 30 | 9 | |
| 70518-3815-3 | Meclizine Hydrochloride | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | 9 | |
| 70518-3815-4 | Meclizine Hydrochloride | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | 9 | |
| 70518-3815-5 | Meclizine Hydrochloride | 10 in 1 BOTTLE, PLASTIC | TABLET | 10 | 9 | |
| 70518-3815-6 | Meclizine Hydrochloride | 20 in 1 BOTTLE, PLASTIC | TABLET | 20 | 9 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-3815 | MECLIZINE HYDROCHLORIDE TABLET [REMEDYREPACK INC.] | 4 | Current NDC, 7 package rows | 20241208_21d4a6ee-0a66-45d7-bab9-c5eef399713d.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70518-3815-1 | EA - Each | 70518-3815 | 67e865a4-66bf-4890-b56d-086dc1935ece | 1 | 2026-02-05 |
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 |
|---|---|---|---|---|---|---|
| Easy Care First Aid Eyewash | WATER | Tender Corporation | a070aac8-e6d2-ef10-e053-2a95a90aa5b1 | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | e07a064b-f680-405c-bbcd-24fac430951e | 2025-11-24 | Warnings | 059QF0KO0R |
| ULINE Eyewash | EYEWASH | Niagara Pharmaceuticals Inc. | 2d7f22d2-320b-6af1-e063-6294a90addc6 | 2025-11-24 | Warnings | 059QF0KO0R |
| Pur-Wash | EYEWASH | Niagara Pharmaceuticals, Inc. | 0d43b1c1-2699-37f1-e054-00144ff88e88 | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | 777e1559-786f-8d54-e053-2991aa0aa98d | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | 7289103a-5cbf-42f4-8848-e827149a43ca | 2025-11-24 | Warnings | 059QF0KO0R |
| Eyewash Additive Concentrate | WATER AND PROPYLENE GLYCOL | Haws Corporation | dd168403-398c-41ff-b1df-d93e4ff39de3 | 2025-11-20 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | Fresenius Kabi USA, LLC | fd823bef-c14c-4708-a18a-8aaa8470412f | 2025-11-18 | Warnings, Adverse reactions | 059QF0KO0R |
| Motion Sickness Relief | MECLIZINE HCL | Rite Aid Corporation | e599dc64-ac10-4f4e-9318-e9fab0526488 | 2025-11-15 | Warnings | 995632 HDP7W44CIO |
| Eyesaline Eyewash Concentrate | PURIFIED WATER | Honeywell Safety Products USA, Inc. | 3765c251-eb14-d60f-e063-6294a90a6a4d | 2025-11-12 | Warnings | 059QF0KO0R |
| Eyesaline Emergency Eyewash | PURIFIED WATER | Honeywell Safety Products USA, Inc. | 37f244fd-c02f-e66a-e063-6394a90aed81 | 2025-11-12 | Warnings | 059QF0KO0R |
| STERILE WATER | WATER | Henry Schein, Inc. | f4087143-9868-4308-b96c-43657ee8ec28 | 2025-11-07 | Warnings, Adverse reactions | 059QF0KO0R |
| Motion Sickness Relief | MECLIZINE HCL | Kroger Company | 64e0496c-5e09-46e9-94b9-624163d71b60 | 2025-11-05 | Warnings | 995666 HDP7W44CIO |
| Motion Sickness Relief | MECLIZINE HCL | Walgreen Company | 27bd9c74-c85e-4eeb-9e43-4120f9001187 | 2025-11-05 | Warnings | 995666 HDP7W44CIO |
| Bacteriostatic Water | BACTERIOSTATIC WATER | ProPharma Distribution | 42c6938e-f747-ae13-e063-6294a90a59a3 | 2025-11-04 | Warnings, Adverse reactions | 059QF0KO0R |
| Sterile Water | WATER | ICU Medical Inc. | aab10f03-26ae-4dbc-a481-ef025e48b405 | 2025-11-02 | Warnings, Adverse reactions | 059QF0KO0R |
| Sterile Water | WATER | ICU Medical Inc. | e3484bc6-ed7f-43ef-9d49-c131a8dff2dd | 2025-11-02 | Warnings, Adverse reactions | 059QF0KO0R |
| MECLIZINE HYDROCHLORIDE | MECLIZINE HYDROCHLORIDE | Bryant Ranch Prepack | 522b55a2-313c-45e8-b1be-07746ada5b0a | 2025-10-31 | Warnings, Adverse reactions | 995624 HDP7W44CIO |
| Sterile Water | WATER | ICU Medical Inc. | 1c0bbcb7-5ed6-4ee7-b297-080d3359474e | 2025-10-29 | Boxed warning, Warnings, Adverse reactions | 059QF0KO0R |
| Bacteriostatic Water | WATER | Henry Schein, Inc. | a833502e-a622-4e81-8c58-cef6ccb6c4c9 | 2025-10-27 | Boxed warning, Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.