NDC 68462-720-84 - drospirenone and ethinyl estradiol
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
- 68462-720
- Requested NDC
- 68462-720-84
- Package NDCs from labels
- 68462-720-84, 68462-720-29
- Manufacturer
- Glenmark Pharmaceuticals Inc., USA | Glenmark Pharmaceuticals Limited
- Effective date
- 2026-01-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| drospirenone and ethinyl estradiol - Glenmark Pharmaceuticals Inc., USA | Glenmark Pharmaceuticals Limited | Glenmark Pharmaceuticals Inc., USA | Glenmark Pharmaceuticals Limited | 2026-01-29 | HUMAN PRESCRIPTION DRUG LABEL |
| drospirenone and ethinyl estradiol - A-S Medication Solutions | A-S Medication Solutions | 2024-05-07 | HUMAN PRESCRIPTION DRUG LABEL |
| drospirenone and ethinyl estradiol - RPK Pharmaceuticals, Inc. | RPK Pharmaceuticals, Inc. | 2023-06-07 | HUMAN PRESCRIPTION DRUG LABEL |
| drospirenone and ethinyl estradiol - Proficient Rx LP | Proficient Rx LP | 2022-07-01 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68462-720-29 | drospirenone and ethinyl estradiol | 3 in 1 CARTON | KIT | 3 | 9 | |
| 68462-720-84 | drospirenone and ethinyl estradiol | 1 in 1 BLISTER PACK | KIT | 1 | 9 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 68462-720-29 | EA - Each | 68462-720 | dbd9d485-9cef-4048-9f32-bf4a90aec60d | 1 | 2015-10-02 |
| 68462-720-84 | EA - Each | 68462-720 | dda11773-efeb-48e8-b0e2-62b020fffea8 | 1 | 2015-10-02 |
DailyMed Socrata Ingredients#
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.