Cryselle
- Product NDC
- 70518-1214
- 11-digit product format
- 705181214
- Labeler code
- 70518
- Product ID
- 70518-1214_6cbe57f7-0db3-58a3-e053-2a91aa0aa871
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Norgestrel and Ethinyl Estradiol
- Dosage form
- KIT
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075840
- Marketing category
- ANDA
- Marketing start
- 2018-05-17
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#