NDC 58160-826-43 - HAVRIX
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
- 58160-826
- Requested NDC
- 58160-826-43
- Package NDCs from labels
- 58160-826-43, 58160-826-52
- Manufacturer
- A-S Medication Solutions
- Effective date
- 2026-09-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| HAVRIX - A-S Medication Solutions | A-S Medication Solutions | 2026-09-21 | VACCINE LABEL |
| HAVRIX - GlaxoSmithKline Biologicals SA | GlaxoSmithKline Biologicals SA | 2026-05-14 | VACCINE LABEL |
| HAVRIX - Dispensing Solutions, Inc. | PSS World Medical, Inc. | Dispensing Solutions, Inc. | PSS World Medical, Inc. | 2013-11-07 | VACCINE LABEL |
| HAVRIX - Dispensing Solutions, Inc. | Dispensing Solutions, Inc. | 2011-10-07 | VACCINE LABEL |
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2013-03-03 | Indexing - Billing Unit |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 58160-826-43 | HAVRIX | 1 mL in 1 SYRINGE | INJECTION, SUSPENSION | 1 | 33 | |
| 58160-826-52 | HAVRIX | 10 in 1 CARTON | INJECTION, SUSPENSION | 10 | 33 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 58160-826-01 | ML - Milliliter | 58160-826 | 3ae3a57f-5ea5-4907-b780-2290fe8d279f | 1 | 2013-03-03 |
| 58160-826-11 | ML - Milliliter | 58160-826 | ef997ed5-9946-46e9-a7ea-fa23409770ae | 1 | 2013-02-13 |
| 58160-826-32 | ML - Milliliter | 58160-826 | 15695cc1-61a5-4c53-a497-dbc00d48c9f6 | 1 | 2013-03-03 |
| 58160-826-43 | ML - Milliliter | 58160-826 | 8d5b9600-232b-44f1-8a17-67fa3ff7346b | 1 | 2013-03-03 |
| 58160-826-52 | ML - Milliliter | 58160-826 | 32246bdf-8c91-4b30-9358-cef0ea8481a1 | 1 | 2013-02-13 |
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 |
|---|---|---|---|---|---|---|
| Claravie | ALUMINUM HYDROXIDE GEL | Gentell LLC | 5afea757-8feb-f907-e063-6394a90a6259 | 2026-09-08 | Warnings | 5QB0T2IUN0 |
| Kroger Extra Strength | ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE | THE KROGER CO., | 175d9f0f-266a-4dc2-865f-d1ebd4ddac51 | 2026-09-01 | Warnings | 5QB0T2IUN0 |
| GERI-LANTA MAXIMUM STRENGTH | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE | Preferred Pharmaceuticals Inc. | 3b049027-30ac-4c78-a4f1-8191f7ed45bf | 2026-08-27 | Warnings | 5QB0T2IUN0 |
| Antacid | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE | Guardian Drug Company | 48ec50ab-f24b-367b-e063-6294a90ad736 | 2026-08-27 | Warnings | 5QB0T2IUN0 |
| REGULAR STRENGTH ANTACID | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE | KROGER COMPANY | b9e61a03-e008-50ab-e053-2a95a90a3210 | 2026-08-26 | Warnings | 5QB0T2IUN0 |
| MAXIMUM STRENGTH ANTACID | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE | CVS PHARMACY | af71e02d-e7c7-f925-e053-2995a90a0861 | 2026-08-26 | Warnings | 5QB0T2IUN0 |
| Antacid | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE | Preferred Pharmaceuticals Inc. | a96496ff-4b35-4ebe-a6e4-bcfa48fb1341 | 2026-08-26 | Warnings | 5QB0T2IUN0 |
| Mag-AL Plus | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, AND SIMETHICONE | PAI Holdings, LLC dba PAI Pharma | 896ab07a-1b40-43ab-8589-3be86b1c4198 | 2026-08-19 | Warnings | 5QB0T2IUN0 |
| CVS Health Extra Strength Antacid | ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE | CVS PHARMACY | 8629529e-4363-4d37-9ae0-27193868df32 | 2026-08-19 | Warnings | 5QB0T2IUN0 |
| CVS Health Extra Strength Heartburn Relief Antacid Original Flavor | ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE | CVS Pharmacy,Inc. | 5c32d90b-68a0-4acf-94b6-d02037cea376 | 2026-08-13 | Warnings | 5QB0T2IUN0 |
| CVS PHARMACY Extra Strength Cherry Flavor | ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE | CVS Pharmacy,Inc. | cf7ae053-fa8d-4e6e-af4f-b846699aaf24 | 2026-08-13 | Warnings | 5QB0T2IUN0 |
| GOOD NEIGHBOR PHARMACY Antacid Extra Strength | ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE | Amerisource Bergen | 5e346dc0-69ce-4cc5-bb5d-bfa833e11c1f | 2026-07-13 | Warnings | 5QB0T2IUN0 |
| Mag-Al Plus | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, AND SIMETHICONE | Cardinal Health 107, LLC | 08df7403-9ee3-4a43-a151-c1a6ef7a7549 | 2026-06-10 | Warnings | 5QB0T2IUN0 |
| ACID GONE ANTACID | ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE | Major Pharmaceuticals | 3d353a92-92f1-4304-8895-31d39dccd88c | 2026-06-01 | Warnings | 5QB0T2IUN0 |
| REGULAR STRENGTH ANTACID/ANTIGAS | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE | NuCare Pharmaceuticals, Inc. | 52e75fe4-f04f-31da-e063-6294a90a1e4f | 2026-05-28 | Warnings | 5QB0T2IUN0 |
| Kesin MAG-AL Plus | ALUMINUM AND MAGNESIUM HYDROXIDE W/SIMETHICONE SUSPENSION | Kesin Pharma Corporation | 436b622a-f028-df98-e063-6394a90a3eaa | 2026-05-08 | Warnings | 5QB0T2IUN0 |
| Kesin MAG-AL Plus XS | ALUMINUM AND MAGNESIUM HYDROXIDE W/SIMETHICONE SUSPENSION | Kesin Pharma Corporation | 436b89f7-e417-0df2-e063-6394a90a96df | 2026-05-08 | Warnings | 5QB0T2IUN0 |
| Kesin MAG-AL | ALUMINUM AND MAGNESIUM HYDROXIDE SUSPENSION | Kesin Pharma Corporation | 42df2198-14dc-da1c-e063-6394a90a1ae6 | 2026-05-08 | Warnings | 5QB0T2IUN0 |
| GERI-LANTA ANTACID ANTIGAS | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE | Preferred Pharmaceuticals Inc. | 27848ae0-3b2f-4bfe-8856-4b8de419091e | 2026-05-06 | Warnings | 5QB0T2IUN0 |
| REGULAR STRENGTH ANTACID | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE | Preferred Pharmaceuticals Inc. | ad3e7ebe-f2a9-4305-b370-59785f5396c8 | 2026-05-06 | Warnings | 5QB0T2IUN0 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.