Orsythia
- Product NDC
- 53002-1647
- 11-digit product format
- 530021647
- Labeler code
- 53002
- Product ID
- 53002-1647_57c8e8c2-6635-421d-a3ef-f6fc26507aac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levonorgestrel and ethinyl estradiol
- Dosage form
- KIT
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA077099
- Marketing category
- ANDA
- Marketing start
- 2011-05-11
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53002-1647-1 | 53002164701 | 1 BLISTER PACK in 1 PACKAGE (53002-1647-1) > 1 KIT in 1 BLISTER PACK * 21 TABLET, FILM COATED in 1 KIT * 7 TABLET, FILM COATED in 1 KIT | 1 blister pack | 2017-09-01 | 0000-00-00 | No | No | Current |
| 53002-1647-3 | 53002164703 | 3 BLISTER PACK in 1 PACKAGE (53002-1647-3) > 1 KIT in 1 BLISTER PACK * 21 TABLET, FILM COATED in 1 KIT * 7 TABLET, FILM COATED in 1 KIT | 3 blister pack | 2017-09-01 | 0000-00-00 | No | No | Current |
| 53002-1647-6 | 53002164706 | 6 BLISTER PACK in 1 PACKAGE (53002-1647-6) > 1 KIT in 1 BLISTER PACK * 21 TABLET, FILM COATED in 1 KIT * 7 TABLET, FILM COATED in 1 KIT | 6 blister pack | 2017-09-01 | 0000-00-00 | No | No | Current |