NDC 70518-3829-01 - FAMOTIDINE
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
- 70518-3829
- Requested NDC
- 70518-3829-01
- Package NDCs from labels
- 70518-3829-0, 70518-3829-1, 70518-3829-2, 70518-3829-3, 70518-3829-4, 70518-3829-5, 70518-3829-6, 70518-3829-7, 70518-3829-8, 70518-3829-9, 70518-3829-01
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-06-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| FAMOTIDINE - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-06-09 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-3829-0 | FAMOTIDINE | 50 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 50 | 13 | |
| 70518-3829-1 | FAMOTIDINE | 30 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 30 | 13 | |
| 70518-3829-2 | FAMOTIDINE | 60 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 60 | 13 | |
| 70518-3829-3 | FAMOTIDINE | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 90 | 13 | |
| 70518-3829-4 | FAMOTIDINE | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 90 | 13 | |
| 70518-3829-5 | FAMOTIDINE | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | 13 | |
| 70518-3829-6 | FAMOTIDINE | 14 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 14 | 13 | |
| 70518-3829-7 | FAMOTIDINE | 60 in 1 BLISTER PACK | TABLET, FILM COATED | 60 | 13 | |
| 70518-3829-8 | FAMOTIDINE | 14 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 14 | 13 | |
| 70518-3829-9 | FAMOTIDINE | 25 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 25 | 13 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-3829 | FAMOTIDINE TABLET, FILM COATED [REMEDYREPACK INC.] | 10 | Current NDC, 10 package rows | 20250115_e59a2c97-19c7-485c-bb1b-272ddb9ae053.zip |
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 |
|---|---|---|---|---|---|---|
| Famotidine | FAMOTIDINE | Family Dollar Stores, Inc. | 0f81e8ac-ddad-13d6-e883-6a5310e058de | 2025-07-17 | Warnings | 310273 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | Discount Drug Mart, Inc | c5d81352-c45b-3ea1-9974-8a096bd05009 | 2025-07-17 | Warnings | 310273 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | Chain Drug Consortium, LLC | 937f7bce-955b-9418-5aed-2e84aee50de3 | 2025-07-17 | Warnings | 310273 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | Chain Drug Marketing Association INC | 1d78bc9e-cf7b-8853-c6dc-b36e5de4dd0a | 2025-07-17 | Warnings | 310273 5QZO15J2Z8 |
| equate famotidine | FAMOTIDINE | WALMART INC. | f38f8a8f-3292-4fe5-b83f-ffd634196d42 | 2025-07-16 | Warnings | 310273 5QZO15J2Z8 |
| Amarte ULTRA VEIL Daily | SUNSCREEN | Amarte USA LLC | 39e9ca98-d0e8-6b8f-e063-6394a90aa366 | 2025-07-15 | Warnings | 15FIX9V2JP |
| Amarte ULTRA VEIL BB Fair | SUNSCREEN | Amarte USA LLC | 39e87950-4103-c2eb-e063-6394a90a0552 | 2025-07-15 | Warnings | 15FIX9V2JP |
| Ibuprofen and famotidine | IBUPROFEN AND FAMOTIDINE | PHOENIX RX LLC | 397f1f23-10c2-569e-e063-6394a90a7164 | 2025-07-11 | Boxed warning, Warnings, Adverse reactions | 5QZO15J2Z8 |
| leader acid reducer complete | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | Cardinal Health 110, LLC. dba Leader | 6a492dd2-61f1-4020-bebd-fcc8e5647207 | 2025-07-08 | Warnings | 5QZO15J2Z8 |
| Dual Action Complete | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | Kroger Company | bf2fcb88-418f-4d5d-85ba-ec165a53ab04 | 2025-07-07 | Warnings | 5QZO15J2Z8 |
| Equate Acid Reducer Complete | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | Wal-Mart Stores Inc | cb683c1c-db81-40a9-9ec5-f8dfa0dcf812 | 2025-07-07 | Warnings | 5QZO15J2Z8 |
| Dual Action Complete | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | H E B | ea712fc4-7f27-4556-b1b8-028f3f6ce57a | 2025-07-07 | Warnings | 5QZO15J2Z8 |
| DG Health acid reducer complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Dolgencorp, LLC | 95c2c515-0f31-49d9-b799-7aaded81a37c | 2025-07-07 | Warnings | 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | Little Pharma, Inc. | 33dc93a5-ee03-2e68-e063-6294a90aeee1 | 2025-07-05 | Warnings | 5QZO15J2Z8 |
| Ibuprofen and famotidine | IBUPROFEN AND FAMOTIDINE | Aurobindo Pharma Limited | 21688404-41fb-487e-8ba0-aea4431a42fa | 2025-07-03 | Boxed warning, Warnings, Adverse reactions | 5QZO15J2Z8 |
| Mineral Lip Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | CAPE COD SKIN CARE CO. INC. | 39093b2d-3fbb-8378-e063-6294a90ac6d8 | 2025-07-03 | 15FIX9V2JP | |
| topcare dual action complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Topco Associates LLC | 8ef70327-9a04-413b-b331-f5d3a94d6b36 | 2025-07-01 | Warnings | 5QZO15J2Z8 |
| Acid Reducer Complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Walgreen Company | 3a456dab-0a2d-4e48-a8e2-e49a7acef963 | 2025-07-01 | Warnings | 5QZO15J2Z8 |
| Dual Action Complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | H E B | c1aa7efa-4be1-4c8f-8994-661dd60e1aa9 | 2025-07-01 | Warnings | 5QZO15J2Z8 |
| leader acid reducer complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Cardinal Health 110, LLC. dba Leader | a5420ef1-313f-4561-baf1-7ae017ea343a | 2025-07-01 | Warnings | 5QZO15J2Z8 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.