Lo-Zumandimine
- Product NDC
- 59651-029
- 11-digit product format
- 596510029
- Labeler code
- 59651
- Product ID
- 59651-029_7bc1835a-cc34-4b65-a6b5-f290aee806b4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Drospirenone and Ethinyl Estradiol
- Dosage form
- KIT
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA209632
- Marketing category
- ANDA
- Marketing start
- 2018-02-27
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lo-Zumandimine
- Listing expiration
- 2026-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 630734, 748797, 748798, 2003375 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59651-029 | LO-ZUMANDIMINE (DROSPIRENONE AND ETHINYL ESTRADIOL) KIT [AUROBINDO PHARMA LIMITED] | 9 | Current NDC, Legacy NDC, 5 package rows | 20231103_a8c718cc-e235-4710-a9e6-6c58433f3028.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 |
|---|
| 59651-029-28 | 59651002928 | 1 in 1 POUCH | | | | | | Historical |
| 59651-029-87 | 59651002987 | 1 POUCH in 1 CARTON (59651-029-87) / 1 BLISTER PACK in 1 POUCH (59651-029-28) / 1 KIT in 1 BLISTER PACK | 1 pouch | 2018-02-27 | 0000-00-00 | No | No | Current |
| 59651-029-88 | 59651002988 | 3 POUCH in 1 CARTON (59651-029-88) / 1 BLISTER PACK in 1 POUCH / 1 KIT in 1 BLISTER PACK | 3 pouch | 2018-02-27 | 0000-00-00 | No | No | Current |