Portia
- Product NDC
- 0555-9020
- 11-digit product format
- 005559020
- Labeler code
- 0555
- Product ID
- 0555-9020_4d63fa4a-ff46-4f2e-b9d5-cab4f5fe1d85
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levonorgestrel and Ethinyl Estradiol
- Dosage form
- KIT
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA075866
- Marketing category
- ANDA
- Marketing start
- 2002-06-27
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Portia
- Listing expiration
- 2026-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 238019, 748797, 748878, 751890 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0555-9020-58 | Portia | 6 in 1 CARTON | KIT | 6 | | 15 |
| 0555-9020-79 | Portia | 1 in 1 POUCH | KIT | 1 | | 15 |
| 0555-9020-79 | Portia | 1 in 1 BLISTER PACK | KIT | 1 | | 15 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0555-9020 | PORTIA (LEVONORGESTREL AND ETHINYL ESTRADIOL) KIT [TEVA PHARMACEUTICALS USA, INC.] | 15 | Current NDC, Legacy NDC, 3 package rows | 20250410_c78b236b-85c4-4258-a524-cea08775100c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0555-9020-58 | 00555902058 | 6 POUCH in 1 CARTON (0555-9020-58) / 1 BLISTER PACK in 1 POUCH (0555-9020-79) / 1 KIT in 1 BLISTER PACK | 6 pouch | 2002-06-27 | 0000-00-00 | No | No | Current |
| 0555-9020-79 | 00555902079 | 1 in 1 POUCH | | | | | | Historical |