NDC 70710-1683-2 - 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
- 70710-1683
- Requested NDC
- 70710-1683-2
- Package NDCs from labels
- 70710-1683-3, 70710-1683-1, 70710-1683-5, 70710-1683-0, 70710-1683-2, 70710-1683-4
- Manufacturer
- Safecor Health, LLC
- Effective date
- 2026-06-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Famotidine - Safecor Health, LLC | Safecor Health, LLC | 2026-06-11 | HUMAN PRESCRIPTION DRUG LABEL |
| Famotidine - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-08-23 | HUMAN PRESCRIPTION DRUG LABEL |
| Famotidine - Preferred Pharmaceuticals Inc. | Preferred Pharmaceuticals Inc. | 2024-04-23 | HUMAN PRESCRIPTION DRUG LABEL |
| Famotidine - Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited | Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited | 2023-10-06 | HUMAN PRESCRIPTION DRUG LABEL |
| Famotidine - NuCare Pharmaceuticals,Inc. | NuCare Pharmaceuticals,Inc. | 2023-05-25 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70710-1683-0 | Famotidine | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | 2 | |
| 70710-1683-1 | Famotidine | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 2 | |
| 70710-1683-2 | Famotidine | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | 2 | |
| 70710-1683-3 | Famotidine | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 2 | |
| 70710-1683-4 | Famotidine | 10 in 1 CARTON | TABLET, FILM COATED | 10 | 2 | |
| 70710-1683-5 | Famotidine | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70710-1683 | FAMOTIDINE TABLET, FILM COATED [ZYDUS PHARMACEUTICALS USA INC.] | 2 | Current NDC, Legacy NDC, 6 package rows | 20231011_b165979b-7ed0-423e-9aeb-2e061df0cd45.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70710-1683-0 | EA - Each | 70710-1683 | 5eb6d531-d787-41c6-9b5e-e7b388dc1aca | 1 | 2022-07-06 |
| 70710-1683-1 | EA - Each | 70710-1683 | 95d40c84-5a37-4de4-8b84-926c70d66eb3 | 1 | 2022-07-06 |
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 |
|---|---|---|---|---|---|---|
| e l f Camo Semi Matte CC SPF 30 Deep 530 W | ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | e.l.f. Cosmetics, Inc. | 940e0b2d-0b10-4534-ba36-e9980cead492 | 2025-10-21 | Warnings | 15FIX9V2JP |
| Clinical Skin Filter Tinted Sunscreen | CLINICAL SKIN FILTER TINTED SUNSCREEN | KRX RESOURCES SDN. BHD. | 22b8856b-671f-def3-e063-6394a90a4ea0 | 2025-10-18 | Warnings | 15FIX9V2JP |
| Clinical Skin Filter Tinted Sunscreen Medium Dark | CLINICAL SKIN FILTER TINTED SUNSCREEN MEDIUM DARK | KRX RESOURCES SDN. BHD. | 22cead37-f862-e859-e063-6394a90a86ce | 2025-10-18 | Warnings | 15FIX9V2JP |
| Krx Aesthetics All Day Glow Sunblocker | KRX AESTHETICS ALL DAY GLOW SUNBLOCKER | KRX RESOURCES SDN. BHD. | 22a60fb9-0fea-92c0-e063-6394a90a088c | 2025-10-18 | Warnings | 15FIX9V2JP |
| Famotidine | FAMOTIDINE | PD-Rx Pharmaceuticals, Inc. | 66f0bf15-ff35-426a-b40c-0d0da79d0861 | 2025-10-16 | Warnings, Adverse reactions | 310273 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | PD-Rx Pharmaceuticals, Inc. | 09ef39a4-c6b3-4395-8211-3f551dc44830 | 2025-10-16 | Warnings, Adverse reactions | 284245 5QZO15J2Z8 |
| DD Cream | DD CREAM | DERMAdoctor, Inc. | 08c9a0cf-ee78-483b-e054-00144ff88e88 | 2025-10-16 | Warnings | 15FIX9V2JP |
| IBUPROFEN AND FAMOTIDINE | IBUPROFEN AND FAMOTIDINE | PHOENIX RX LLC | 3ff33400-30e8-87fa-e063-6394a90a7f5c | 2025-10-15 | Boxed warning, Warnings, Adverse reactions | 5QZO15J2Z8 |
| Ciele Filter and Protect | TITANIUM DIOXIDE, ZINC OXIDE | Ciele | 0309b0ef-baca-b41d-e063-6294a90a49d7 | 2025-10-15 | Warnings | 15FIX9V2JP |
| Defend and Balance TInted Mineral Sunscreen SPF 50 | SUNSCREEN | Epicuren Discovery | 41367f05-59d8-6736-e063-6394a90a5f17 | 2025-10-15 | Warnings | 15FIX9V2JP |
| Famotidine | FAMOTIDINE | PD-Rx Pharmaceuticals, Inc. | 5798d282-ce83-49aa-bc33-13203f2b5285 | 2025-10-15 | Warnings, Adverse reactions | 284245 5QZO15J2Z8 |
| acid reducer complete | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | Safeway | 4f0a178c-d0ed-4bbc-a8ce-fda3789d25f0 | 2025-10-14 | Warnings | 5QZO15J2Z8 |
| DENTI BUONGIORNO PEACH MINT WHITENING TOOTH | HYDROGEN PEROXIDE, SILICA | ATOSAFE CO., Ltd | 41196c2f-8e2e-a54d-e063-6294a90ad8a7 | 2025-10-14 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO PEACH MINT WHITENING TOOTH | HYDROGEN PEROXIDE, SILICA | DONG IL PHARMS CO.,LTD | 41198822-7c8f-ceb2-e063-6394a90a4373 | 2025-10-14 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO ORIGINAL TOOTH | SILICA, SODIUM MONOFLUOROPHOSPHATE | DONG IL PHARMS CO.,LTD | 41197bb6-f6f4-c86d-e063-6294a90ad476 | 2025-10-14 | Warnings | ETJ7Z6XBU4 |
| Famotidine | FAMOTIDINE | PD-Rx Pharmaceuticals, Inc. | 2f5ec69d-926c-47a2-be47-8fef2e0ff207 | 2025-10-14 | Warnings, Adverse reactions | 284245 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | Bryant Ranch Prepack | c133a9e1-ca48-4ee2-8768-01f44f5dd511 | 2025-10-14 | Warnings, Adverse reactions | 310273 5QZO15J2Z8 |
| Skinlycious Multi Protection Mineral Sunscreen Broad Spectrum SPF 30 | TITANIUM DIOXIDE , ZINC OXIDE | Skinlycious Pte Ltd | e0ad02c3-f5ed-4b72-ba96-07d9c489a4ea | 2025-10-13 | Warnings | 15FIX9V2JP |
| DENTI BUONGIORNO ORIGINAL TOOTH | SILICA, SODIUM MONOFLUOROPHOSPHATE | ATOSAFE CO., Ltd | 4114ab09-1115-6b0b-e063-6394a90ab442 | 2025-10-13 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO PLAQUE CARE TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE | ATOSAFE CO., Ltd | 41155922-d7ac-0a7a-e063-6294a90afe48 | 2025-10-13 | Warnings | ETJ7Z6XBU4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.