NDC 75907-215 - SRONYX
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
- 75907-215
- Manufacturer
- Dr. Reddy's Labratories Inc.
- Effective date
- 2024-09-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| SRONYX ® (Levonorgestrel and Ethinyl Estradiol Tablets USP) | Dr. Reddy's Labratories Inc. | 2024-09-20 | HUMAN PRESCRIPTION DRUG LABEL |
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 |
|---|---|---|---|---|---|---|
| Quality Choice Moisturizing Relief Eye Drops | DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL | Chain Drug Marketing Association, Inc. | 1fb81759-5931-59c8-e063-6294a90a2277 | 2025-12-30 | Warnings | FZ989GH94E |
| Her Style | LEVONORGESTREL | Ingenus Pharmaceuticals, LLC | 6e631755-b7c5-4a3a-b46d-f66b4ceedb1c | 2025-12-05 | Warnings | 5W7SIA7YZW |
| New Day | LEVONORGESTREL | Northstar Rx LLC | 9e8c96f6-ab51-4721-b276-1ca02a712510 | 2025-12-05 | Warnings | 5W7SIA7YZW |
| My Way | LEVONORGESTREL | Lupin Pharmaceuticals, Inc. | 3efec61d-e0a6-49c5-9b88-834db6d171fd | 2025-12-02 | Warnings | 5W7SIA7YZW |
| Julie Morning After Pill | LEVONORGESTREL | Julie Products Inc. | 40bb96f0-d5f1-1ec3-e063-6294a90a74b1 | 2025-11-26 | Warnings | 5W7SIA7YZW |
| Julie Morning After Pill | LEVONORGESTREL | Julie Products Inc. | 40bbad6f-0c54-e4ed-e063-6394a90af3ad | 2025-11-14 | Warnings | 5W7SIA7YZW |
| NuvaRing | ETONOGESTREL AND ETHINYL ESTRADIOL | Organon LLC | 55eb60e3-6f4d-40a3-8ee6-e7fd2d0c7d97 | 2025-11-14 | Boxed warning, Warnings, Adverse reactions | 423D2T571U |
| Mirena | LEVONORGESTREL | Bayer HealthCare Pharmaceuticals Inc. | dcbd6aa2-b3fa-479a-a676-56ea742962fc | 2025-10-29 | Warnings, Adverse reactions | 5W7SIA7YZW |
| LACRIFRESH HYDRAPF | GLYCERIN, POVIDONE | AVIZOR, S.A. | 41bbd23e-0ec8-eb18-e063-6294a90a46d1 | 2025-10-27 | Warnings | FZ989GH94E |
| LACRIFRESH HYDRAMAXPF | GLYCERIN, POVIDONE | AVIZOR, S.A. | 41be1604-89b4-7ec3-e063-6294a90a3331 | 2025-10-27 | Warnings | FZ989GH94E |
| Stye | POLYVINYL ALCOHOL AND POVIDONE | Medtech Products Inc. | 60c11d3d-df20-4d1c-b425-49a84fecea30 | 2025-10-23 | Warnings | FZ989GH94E |
| Kyleena | LEVONORGESTREL | Bayer HealthCare Pharmaceuticals Inc. | 2e07c155-21e1-4781-9633-ce8bddd47080 | 2025-10-23 | Warnings, Adverse reactions | 5W7SIA7YZW |
| iVIZIA Dry Eye | POVIDONE | Thea Pharma Inc. | 1ef73cb1-da48-a713-e063-6294a90afa9d | 2025-10-20 | Warnings | FZ989GH94E |
| NUVARING | ETONOGESTREL AND ETHINYL ESTRADIOL | A-S Medication Solutions | 524c7188-ee84-4d5c-a6ab-e7a5ae36e22b | 2025-10-01 | Boxed warning, Warnings, Adverse reactions | 423D2T571U |
| Eyes Irritation Relief | POLYVINYL ALCOHOL AND POVIDONE AND TETRAHYDROZOLINE HYDROCHLORIDE | CARDINAL HEALTH 110, LLC. DBA LEADER | bd2608c6-ffdf-352a-e053-2995a90a26a8 | 2025-09-12 | Warnings | FZ989GH94E |
| 3a85c443-f500-b2c9-e063-6294a90abf52 | 7f89a3b5-22b6-173d-8ad2-e3fabb621a64 | 2025-07-22 | Boxed warning, Warnings, Adverse reactions | 7f89a3b5-22b6-173d-8ad2-e3fabb621a64 | ||
| Julie | LEVONORGESTREL | Julie Products Inc | 2e9784da-2186-a630-e063-6294a90a8493 | 2025-07-14 | Warnings | 5W7SIA7YZW |
| Levonorgestrel | LEVONORGESTREL | Ohm Laboratories Inc. | f3f2a41a-a9af-4d63-81d8-33181d12af40 | 2025-07-04 | Warnings | 5W7SIA7YZW |
| AfterPill | LEVONORGESTREL | Syzygy Healthcare Solutions, LLC PO Box 588, Westport, CT 06880 | 4d284ba4-9cd7-48e4-95b9-cd6d0367bfd1 | 2025-05-01 | Warnings | 5W7SIA7YZW |
| PostDay One-Step | LEVONORGESTREL | Home Health Brands, LLC | 01c8c95c-6fbe-4068-915d-74418a6bb570 | 2025-04-23 | Warnings | 5W7SIA7YZW |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.