NDC 70710-1684-2 - 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
- 70710-1684
- Requested NDC
- 70710-1684-2
- Package NDCs from labels
- 70710-1684-3, 70710-1684-1, 70710-1684-5, 70710-1684-0, 70710-1684-2, 70710-1684-4
- Manufacturer
- St. Mary's Medical Park Pharmacy
- Effective date
- 2026-06-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Famotidine - St. Mary's Medical Park Pharmacy | St. Mary's Medical Park Pharmacy | 2026-06-02 | HUMAN PRESCRIPTION DRUG LABEL |
| Famotidine - NuCare Pharmaceuticals,Inc. | NuCare Pharmaceuticals,Inc. | 2025-02-03 | 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 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70710-1684-0 | Famotidine | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | 2 | |
| 70710-1684-1 | Famotidine | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 2 | |
| 70710-1684-2 | Famotidine | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | 2 | |
| 70710-1684-3 | Famotidine | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 2 | |
| 70710-1684-4 | Famotidine | 10 in 1 CARTON | TABLET, FILM COATED | 10 | 2 | |
| 70710-1684-5 | Famotidine | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70710-1684 | 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 |
|---|---|---|---|---|---|
| 70710-1684-0 | EA - Each | 70710-1684 | d8d62b14-b7e9-4404-8adb-3ce0ac082a3d | 1 | 2022-07-06 |
| 70710-1684-1 | EA - Each | 70710-1684 | 08d5da86-6ab6-48a7-b00c-976959c0accf | 1 | 2022-07-06 |
| 70710-1684-5 | EA - Each | 70710-1684 | ac073ac9-04b3-4258-8f27-54f9af245950 | 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 |
|---|---|---|---|---|---|---|
| Meijer Baby Tear Free SPF 50 | TITANIUM DIOXIDE, ZINC OXIDE | Meijer Distributing Inc. | 2434de23-bcc9-4a83-9945-16fc3f2b8c61 | 2016-06-01 | Warnings | 15FIX9V2JP |
| TOTAL DEFENSE REPAIR BROAD SPECTRUM SPF 34 Sunscreen (Tinted) | OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE AND ZINC OXIDE | Allergan, Inc. | 6a996e03-907f-4e6a-b232-0892b86956b0 | 2015-08-21 | Warnings | 15FIX9V2JP |
| Renewal Firming Day Broad Spectrum SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | BURT'S BEES, INC. | 18ceb5d8-4b76-6a54-e054-00144ff88e88 | 2015-06-18 | Warnings | 15FIX9V2JP |
| TiZO2 | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals, LTD. | 30468afc-9616-4765-b046-12e97a0a7827 | 2010-12-20 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.