Zenchent FE
- Product NDC
- 69238-1581
- 11-digit product format
- 692381581
- Labeler code
- 69238
- Product ID
- 69238-1581_44ee7abe-a384-4540-82e8-55c44c05863e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Norethindrone and Ethinyl Estradiol
- Dosage form
- KIT
- Route
- ORAL
- Labeler
- Amneal Pharmaceuticals NY LLC
- Application
- ANDA078892
- Marketing category
- ANDA
- Marketing start
- 2018-06-29
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Zenchent FE
- Listing expiration
- 2026-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 433718, 1095223, 1095224, 1483558 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69238-1581-3 | Zenchent FE | 3 in 1 CARTON | KIT | 3 | | 7 |
| 69238-1581-3 | Zenchent FE | 1 in 1 BLISTER PACK | KIT | 1 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69238-1581 | ZENCHENT FE (NORETHINDRONE AND ETHINYL ESTRADIOL) KIT [AMNEAL PHARMACEUTICALS NY LLC] | 7 | Current NDC, Legacy NDC, 2 package rows | 20231231_17a9750b-e1b0-4293-992d-195b2eb9ea11.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 |
|---|
| 69238-1581-3 | 69238158103 | 3 BLISTER PACK in 1 CARTON (69238-1581-3) / 1 KIT in 1 BLISTER PACK | 3 blister pack | 2018-06-29 | 0000-00-00 | No | No | Current |