NDC 16571-757-50 - escitalopram
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
- 16571-757
- Requested NDC
- 16571-757-50
- Package NDCs from labels
- 16571-757-01, 16571-757-10, 16571-757-50
- Manufacturer
- Rising Pharma Holdings, Inc. | Graviti Pharmaceuticals Private Limited
- Effective date
- 2026-10-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| escitalopram - Rising Pharma Holdings, Inc. | Graviti Pharmaceuticals Private Limited | Rising Pharma Holdings, Inc. | Graviti Pharmaceuticals Private Limited | 2026-10-03 | HUMAN PRESCRIPTION DRUG LABEL |
| escitalopram - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-09-01 | HUMAN PRESCRIPTION DRUG LABEL |
| escitalopram - Preferred Pharmaceuticals Inc. | Preferred Pharmaceuticals Inc. | 2026-04-13 | HUMAN PRESCRIPTION DRUG LABEL |
| escitalopram - Coupler LLC | Graviti Pharmaceuticals Private Limited | Coupler LLC | Graviti Pharmaceuticals Private Limited | 2025-02-04 | HUMAN PRESCRIPTION DRUG LABEL |
| escitalopram - Quality Care Products, LLC | Quality Care Products, LLC | 2024-12-19 | HUMAN PRESCRIPTION DRUG LABEL |
| escitalopram - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-12-11 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 16571-757-01 | escitalopram | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 2 | |
| 16571-757-10 | escitalopram | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | 2 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 16571-757-01 | EA - Each | 16571-757 | 4985aa08-e56a-4eca-a610-0efde4165b89 | 1 | 2023-07-06 |
| 16571-757-10 | EA - Each | 16571-757 | 95823914-ea05-4cbf-983d-e497aa161ba4 | 1 | 2023-07-06 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.