Drospirenone and ethinyl estradiol
- Product NDC
- 60505-4183
- 11-digit product format
- 605054183
- Labeler code
- 60505
- Product ID
- 60505-4183_9e6d8cb9-7833-5939-0a9c-9dc3fb7eb41b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Drospirenone and ethinyl estradiol
- Dosage form
- KIT
- Route
- ORAL
- Labeler
- Apotex Corp.
- Application
- ANDA205876
- Marketing category
- ANDA
- Marketing start
- 2018-03-20
- Marketing end
- 2021-08-21
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60505-4183-3 | 60505418303 | 1 KIT in 1 CARTON (60505-4183-3) * 21 TABLET, FILM COATED in 1 BLISTER PACK * 7 TABLET, FILM COATED in 1 BLISTER PACK | 1 kit | 2018-03-20 | 2021-08-21 | No | No | Current |