NDC 63672-0044 - Amlodipine Besylate
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
- 63672-0044
- Package NDCs from labels
- 63672-0044-3
- Manufacturer
- Synthon Pharmaceuticals, Inc.
- Effective date
- 2008-01-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Amlodipine Besylate Tablets | Synthon Pharmaceuticals, Inc. | 2008-01-23 | HUMAN PRESCRIPTION DRUG LABELING |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63672-0044-3 | Amlodipine Besylate | 90 in 1 BOTTLE | TABLET | 90 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 63672-0044 | AMLODIPINE BESYLATE (AMLODIPINE BESYLATE) TABLET [SYNTHON PHARMACEUTICALS, INC.] | 1 | 1 package rows | 20080130_6E9A6C82-9F25-4C71-B09A-929BD5D7B1CF.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63672-0044-3 | EA - Each | 63672-0044 | 50b13dd6-34bc-4a84-9ecf-c5b53b40abf9 | 1 | 2015-10-02 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Amlodipine besylate | ACTIVE INGREDIENT | 864V2Q084H | AMLODIPINE BESYLATE (AMLODIPINE BESYLATE) TABLET [SYNTHON PHARMACEUTICALS, INC.] | 1 | |
| Amlodipine | ACTIVE MOIETY | 1J444QC288 | AMLODIPINE BESYLATE (AMLODIPINE BESYLATE) TABLET [SYNTHON PHARMACEUTICALS, INC.] | 1 | |
| magnesium stearate | INACTIVE INGREDIENT | 70097M6I30 | AMLODIPINE BESYLATE (AMLODIPINE BESYLATE) TABLET [SYNTHON PHARMACEUTICALS, INC.] | 1 | |
| microcrystalline cellulose | INACTIVE INGREDIENT | AMLODIPINE BESYLATE (AMLODIPINE BESYLATE) TABLET [SYNTHON PHARMACEUTICALS, INC.] | 1 | ||
| sodium starch glycolate | INACTIVE INGREDIENT | AMLODIPINE BESYLATE (AMLODIPINE BESYLATE) TABLET [SYNTHON PHARMACEUTICALS, INC.] | 1 |
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 |
|---|---|---|---|---|---|---|
| AMLODIPINE BESYLATE | AMLODIPINE BESYLATE | Proficient Rx LP | 410aa0a5-43cf-455c-b51d-7dfbc24eee32 | 2020-02-01 | Warnings, Adverse reactions | 308135 |
| Norvasc | AMLODIPINE BESYLATE | PFIZER LABORATORIES DIV PFIZER INC | abd6a2ca-40c2-485c-bc53-db1c652505ed | 2019-01-15 | Warnings, Adverse reactions | 197361 308136 308135 |
| Amlodipine besylate | AMLODIPINE BESYLATE | Aphena Pharma Solutions - Tennessee, LLC | 17e6d552-7528-4597-9498-104cb04f32e7 | 2017-10-25 | Warnings, Adverse reactions | 308135 |
| 7ABC4DB9-AADA-7A24-9BF4-DC0D0B06E180 | 6E9A6C82-9F25-4C71-B09A-929BD5D7B1CF | 2008-01-23 | Warnings, Adverse reactions | 7ABC4DB9-AADA-7A24-9BF4-DC0D0B06E180 6E9A6C82-9F25-4C71-B09A-929BD5D7B1CF |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.