NDC 60219-2149-01 - Bimatoprost
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
- 60219-2149
- Requested NDC
- 60219-2149-01
- Package NDCs from labels
- 60219-2149-1, 60219-2149-4, 60219-2149-2, 60219-2149-01
- Manufacturer
- Amneal Pharmaceuticals NY LLC | Amneal Pharmaceuticals Private Limited
- Effective date
- 2025-05-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Bimatoprost - Amneal Pharmaceuticals NY LLC | Amneal Pharmaceuticals Private Limited | Amneal Pharmaceuticals NY LLC | Amneal Pharmaceuticals Private Limited | 2025-05-24 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 60219-2149-1 | Bimatoprost | 2.5 mL in 1 BOTTLE | SOLUTION/ DROPS | 2.5 | 4 | |
| 60219-2149-1 | Bimatoprost | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | 4 | |
| 60219-2149-2 | Bimatoprost | 7.5 mL in 1 BOTTLE | SOLUTION/ DROPS | 7.5 | 4 | |
| 60219-2149-2 | Bimatoprost | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | 4 | |
| 60219-2149-4 | Bimatoprost | 5 mL in 1 BOTTLE | SOLUTION/ DROPS | 5 | 4 | |
| 60219-2149-4 | Bimatoprost | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | 4 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 60219-2149-1 | ML - Milliliter | 60219-2149 | 044c816b-8a94-4d40-9f07-116532cdfc0f | 1 | 2026-04-20 |
| 60219-2149-2 | ML - Milliliter | 60219-2149 | a115007b-c038-4572-a7a9-f57f8546240e | 1 | 2026-04-20 |
| 60219-2149-4 | ML - Milliliter | 60219-2149 | 1afbd3a2-4446-4014-8d9e-0fbcdb85e5ff | 1 | 2026-04-20 |
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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.