AUBRA
- Product NDC
- 53002-1692
- 11-digit product format
- 530021692
- Labeler code
- 53002
- Product ID
- 53002-1692_d4b944c8-7e66-456b-a6fb-d9f8844a9891
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levonorgestrel and Ethinyl Estradiol
- Dosage form
- KIT
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA200245
- Marketing category
- ANDA
- Marketing start
- 2013-10-15
- 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#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 53002-1692-1 | 2020-12-16 | C162847 | 48780-1 | 9d75b9d0-bbcf-f424-e053-dadaa90a57ce | 7cff92f9-eaec-4982-8f25-2e1596fb2fb2 |
| 53002-1692-3 | 2020-12-16 | C162847 | 48780-1 | 9d75b9d0-bbcf-f424-e053-dadaa90a57ce | 7cff92f9-eaec-4982-8f25-2e1596fb2fb2 |
| 53002-1692-6 | 2020-12-16 | C162847 | 48780-1 | 9d75b9d0-bbcf-f424-e053-dadaa90a57ce | 7cff92f9-eaec-4982-8f25-2e1596fb2fb2 |
| 53002-1692-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-bbcf-f424-e053-dadaa90a57ce | 7cff92f9-eaec-4982-8f25-2e1596fb2fb2 |
| 53002-1692-3 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-bbcf-f424-e053-dadaa90a57ce | 7cff92f9-eaec-4982-8f25-2e1596fb2fb2 |
| 53002-1692-6 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-bbcf-f424-e053-dadaa90a57ce | 7cff92f9-eaec-4982-8f25-2e1596fb2fb2 |