NDC 70700-808 - VIENVA TM
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
- 70700-808
- Manufacturer
- A-S Medication Solutions
- Effective date
- 2026-03-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| VIENVA TM - A-S Medication Solutions | A-S Medication Solutions | 2026-03-03 | HUMAN PRESCRIPTION DRUG LABEL |
| Vienva - Xiromed, LLC. | XIROMED PHARMA ESPANA, S.L. | Xiromed, LLC. | XIROMED PHARMA ESPANA, S.L. | 2024-11-11 | 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 |
|---|---|---|---|---|---|---|
| AfterPlan | LEVONORGESTREL | SUN PHARMACEUTICAL INDUSTRIES, INC. | c30c7bc2-04fa-4590-96f5-5bcf4bba3f1a | 2018-10-26 | Warnings | 5W7SIA7YZW |
| Morning After | LEVONORGESTREL | Rapha Pharmaceuticals, Inc. | 677aa953-3c30-4ce5-e053-2991aa0ab2b2 | 2018-03-15 | Warnings | 5W7SIA7YZW |
| Levonorgestrel | LEVONORGESTREL | Novel Laboratories, Inc. | ac13a073-a33a-45f7-8483-eecc9190195f | 2017-09-15 | 5W7SIA7YZW | |
| Tri Femynor | NORGESTIMATE AND ETHINYL ESTRADIOL | Amneal Pharmaceuticals NY LLC | 46bbdf70-2b80-4359-a19b-d94ff99eac98 | 2016-08-30 | Boxed warning, Warnings, Adverse reactions | 748797 |
| My Way | LEVONORGESTREL | Lupin Pharmaceuticals,Inc. | ec01077e-ac3c-424a-9edc-0854fe0a2e0d | 2016-06-17 | Warnings | 5W7SIA7YZW |
| Femynor | NORGESTIMATE AND ETHINYL ESTRADIOL | Amneal Pharmaceuticals NY LLC | 59bce25b-ee2c-4f06-afff-e5141d063602 | 2016-05-30 | Boxed warning, Warnings, Adverse reactions | 748797 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.