Ogestrel
- Product NDC
- 52544-848
- 11-digit product format
- 525440848
- Labeler code
- 52544
- Product ID
- 52544-848_04dfe658-5e97-4c06-96d8-6f3eb0061f57
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Norgestrel and Ethinyl Estradiol
- Dosage form
- KIT
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA075406
- Marketing category
- ANDA
- Marketing start
- 2000-08-21
- Marketing end
- 2020-11-30
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 52544-848-28 | EA - Each | 52544-848 | 65035674-9092-4331-83dc-a0750ca9bd7b | 1 | 2012-07-24 |