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 |
|---|---|---|---|---|---|---|
| Motion Sickness Relief | MECLIZINE HCL | L.N.K. International, Inc. | 8e1889de-fbef-44f1-bbfb-c68a78e6330c | 2026-07-30 | Warnings | 995666 HDP7W44CIO |
| DECONIMO Reconstitution | DECONIMO RECONSTITUTION | Image Amazon LLC | 57ab9b1c-9a18-3786-e063-6394a90a2c63 | 2026-07-28 | Warnings | 059QF0KO0R |
| MECLIZINE HYDROCHLORIDE | MECLIZINE | Bryant Ranch Prepack | dab43efd-bec6-472f-b13a-1c043914dcd1 | 2026-07-27 | Warnings, Adverse reactions | 995666 HDP7W44CIO |
| Sterile Water | WATER | Cardinal Health 107, LLC | 9655cd02-82b5-4a75-813b-854b19551481 | 2026-07-21 | Warnings, Adverse reactions | 059QF0KO0R |
| Meclizine Hydrochloride | MECLIZINE HYDROCHLORIDE | Rugby Laboratories | b57f14a7-3852-03db-e053-2a95a90a80d6 | 2026-07-16 | Warnings | 995632 HDP7W44CIO |
| Meclizine Hydrochloride | MECLIZINE HYDROCHLORIDE | Northwind Health Company, LLC | 1b541252-e8a7-b678-e063-6394a90a34dc | 2026-07-14 | Warnings, Adverse reactions | 995666 HDP7W44CIO |
| Motion Sickness Relief | MECLIZINE HCL | Topco Associates, LLC | 307e3144-3b01-4bd0-9155-6b58fc4cab92 | 2026-07-09 | Warnings | 995666 HDP7W44CIO |
| 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 | 059QF0KO0R |
| MECLIZINE HYDROCHLORIDE | MECLIZINE HYDROCLORIDE | REMEDYREPACK INC. | ba2fb6de-af86-4c05-9018-135e1f8594f9 | 2026-07-03 | Warnings, Adverse reactions | 995666 HDP7W44CIO |
| Eyesaline Eyewash Concentrate | PURIFIED WATER | Protective Industrial Products, Inc. | 558e5926-9027-d3f6-e063-6294a90ab121 | 2026-07-02 | Warnings | 059QF0KO0R |
| Fendall 2000 Pure Flow | PURIFIED WATER | Protective Industrial Products, Inc. | 55a1d07e-0006-0c75-e063-6394a90a7acc | 2026-07-02 | Warnings | 059QF0KO0R |
| Fendall 1000 Pure Flow | PURIFIED WATER | Protective Industrial Products, Inc. | 55a2f4da-bb1e-8ead-e063-6394a90af72e | 2026-07-02 | Warnings | 059QF0KO0R |
| Sterile Eyesaline Eyewash | STERILE EYESALINE EYEWASH | Protective Industrial Products, Inc. | 55a290e8-8310-8be4-e063-6394a90abdce | 2026-07-02 | Warnings | 059QF0KO0R |
| Eyesaline Emergency Eyewash | PURIFIED WATER | Protective Industrial Products, Inc. | 55a261c2-725d-6765-e063-6294a90a3260 | 2026-07-02 | Warnings | 059QF0KO0R |
| Remodulin | TREPROSTINIL | United Therapeutics Corporation | 6c80bb38-e8db-4138-9f0d-dbbf9c673185 | 2026-07-02 | Warnings, Adverse reactions | 059QF0KO0R |
| SET 4TE HOMO | ADEPS SUILLUS, BRYONIA (ALBA), CALCAREA PHOSPHORICA, CHOLINUM, DNA, DOPAMINE (HYDROCHLORIDE), FERRUM PHOSPHORICUM, FOLIC ACID, INSULINUM (HUMAN), LEPTIN, MAGNESIA MURIATICA, L-METHIONINE, METHYLCOBALAMIN, PROTEUS (VULGARIS), RHUS TOX, RIBOFLAVINUM, RUTA GRAVEOLENS, SACCHARUM OFFICINALE, THIOSINAMINUM, ZINCUM METALLICUM | Deseret Biologicals, Inc. | e7b8d75b-f2bc-4013-91e7-bf5bbec11a90 | 2026-06-25 | Warnings | C151H8M554 |
| MECLIZINE HYDROCHLORIDE | MECLIZINE | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | b11c10b9-f40e-4ea7-9c5d-118517049f9d | 2026-06-25 | Warnings, Adverse reactions | 995686 HDP7W44CIO |
| Fendall 2000 Pure Flow | PURIFIED WATER | Honeywell Safety Products USA, Inc. | 37dead3e-60cb-88ae-e063-6294a90a8f70 | 2026-06-24 | Warnings | 059QF0KO0R |
| Bacteriostatic Water | BACTERIOSTATIC WATER | Fujian Genohope Biotech Ltd. | 54f66b82-c9e5-a2bc-e063-6394a90adbbc | 2026-06-23 | 059QF0KO0R | |
| DRAMAMINE CHEWABLE ORANGE | MECLIZINE HYDROCHLORIDE | Medtech Products Inc. | 30387e63-278d-412a-bcad-7965c7c0aea7 | 2026-06-23 | Warnings | 995632 HDP7W44CIO |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.