NDC 49427-343 - RECONCILE
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
- 49427-343
- Package NDCs from labels
- 49427-343-57, 49427-343-44
- Manufacturer
- Pegasus Laboratories, Inc.
- Effective date
- 2022-12-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| RECONCILE - Pegasus Laboratories, Inc. | Pegasus Laboratories, Inc. | 2022-12-29 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49427-343-44 | RECONCILE | 90 in 1 BOTTLE | TABLET, CHEWABLE | 90 | 3 | |
| 49427-343-57 | RECONCILE | 30 in 1 BOTTLE | TABLET, CHEWABLE | 30 | 3 |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| Fluoxetine | FLUOXETINE HYDROCHLORIDE | Proficient Rx LP | 0cba1992-3990-42a1-9d9a-77b593bbb02e | 2019-10-01 | Boxed warning, Warnings, Adverse reactions | I9W7N6B1KJ |
| Fluoxetine | FLUOXETINE HYDROCHLORIDE | Bryant Ranch Prepack | 02283de9-6087-45f7-a9ce-3b082ce860de | 2019-02-01 | Boxed warning, Warnings, Adverse reactions | I9W7N6B1KJ |
| Fluoxetine | FLUOXETINE HYDROCHLORIDE | Vensun Pharmaceuticals, Inc. | b4f37ef1-8f5e-4318-90f1-2d8f8afb669c | 2017-09-18 | Boxed warning, Warnings, Adverse reactions | I9W7N6B1KJ |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.