Escitalopram
- Product NDC
- 68071-4332
- 11-digit product format
- 680714332
- Labeler code
- 68071
- Product ID
- 68071-4332_674ecbc3-61b9-b65e-e053-2a91aa0aadc9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA076765
- Marketing category
- ANDA
- Marketing start
- 2012-03-14
- Marketing end
- 0000-00-00
- Substance
- ESCITALOPRAM OXALATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68071-4332-2 | 2020-06-15 | C162847 | 48780-1 | 9d75b9d0-edc7-f424-e053-dadaa90a57ce | 674ecbc3-61b8-b65e-e053-2a91aa0aadc9 |
| 68071-4332-3 | 2020-06-15 | C162847 | 48780-1 | 9d75b9d0-edc7-f424-e053-dadaa90a57ce | 674ecbc3-61b8-b65e-e053-2a91aa0aadc9 |
| 68071-4332-9 | 2020-06-15 | C162847 | 48780-1 | 9d75b9d0-edc7-f424-e053-dadaa90a57ce | 674ecbc3-61b8-b65e-e053-2a91aa0aadc9 |
| 68071-4332-2 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-edc7-f424-e053-dadaa90a57ce | 674ecbc3-61b8-b65e-e053-2a91aa0aadc9 |
| 68071-4332-3 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-edc7-f424-e053-dadaa90a57ce | 674ecbc3-61b8-b65e-e053-2a91aa0aadc9 |
| 68071-4332-9 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-edc7-f424-e053-dadaa90a57ce | 674ecbc3-61b8-b65e-e053-2a91aa0aadc9 |