Levonorgestrel and Ethinyl Estradiol
- Product NDC
- 60505-4899
- 11-digit product format
- 605054899
- Labeler code
- 60505
- Product ID
- 60505-4899_4e915bff-15ff-1cf4-e063-6294a90ae7c3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levonorgestrel and Ethinyl Estradiol
- Dosage form
- KIT
- Labeler
- Apotex Corp.
- Application
- ANDA207033
- Marketing category
- ANDA
- Marketing start
- 2026-04-03
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Levonorgestrel and Ethinyl Estradiol
- Listing expiration
- 2027-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 238019, 748797, 748878 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60505-4899-8 | Levonorgestrel and Ethinyl Estradiol | 1 in 1 BLISTER PACK | KIT | 1 | | 1 |
| 60505-4899-8 | Levonorgestrel and Ethinyl Estradiol | 3 in 1 CARTON | KIT | 3 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60505-4899-8 | 60505489908 | 3 BLISTER PACK in 1 CARTON (60505-4899-8) / 1 KIT in 1 BLISTER PACK | 3 blister pack | 2026-04-03 | No | No | Historical |