Fexofenadine HCl
- Product NDC
- 55700-500
- 11-digit product format
- 557000500
- Labeler code
- 55700
- Product ID
- 55700-500_9f9f638e-af33-43fd-8a6b-c4d886105d06
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA204507
- Marketing category
- ANDA
- Marketing start
- 2015-09-16
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 55700-500-30 | 2025-01-09 | C162847 | 48780-1 | ba0f9c33-33fc-a910-e053-dadaa90a0b85 | 8f69403b-2059-48c2-86be-d5a0234429c0 |
| 55700-500-60 | 2025-01-09 | C162847 | 48780-1 | ba0f9c33-33fc-a910-e053-dadaa90a0b85 | 8f69403b-2059-48c2-86be-d5a0234429c0 |
| 55700-500-90 | 2025-01-09 | C162847 | 48780-1 | ba0f9c33-33fc-a910-e053-dadaa90a0b85 | 8f69403b-2059-48c2-86be-d5a0234429c0 |
| 55700-500-30 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-33fc-a910-e053-dadaa90a0b85 | 8f69403b-2059-48c2-86be-d5a0234429c0 |
| 55700-500-60 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-33fc-a910-e053-dadaa90a0b85 | 8f69403b-2059-48c2-86be-d5a0234429c0 |
| 55700-500-90 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-33fc-a910-e053-dadaa90a0b85 | 8f69403b-2059-48c2-86be-d5a0234429c0 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 55700-500-30 | EA - Each | 55700-500 | 36011d41-7c68-418d-a026-001e96358e00 | 1 | 2017-03-06 |
| 55700-500-60 | EA - Each | 55700-500 | b89ba611-d653-483f-9313-a0ce3d36cc75 | 1 | 2018-01-12 |
| 55700-500-90 | EA - Each | 55700-500 | 1d3517b9-f8de-40cd-b8ff-7911a47e2d34 | 1 | 2018-02-20 |