Allergy Relief
- Product NDC
- 59726-505
- 11-digit product format
- 597260505
- Labeler code
- 59726
- Product ID
- 59726-505_20e09a91-78b1-4a99-a6d2-473451495f40
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine HCl
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- ANDA204507
- Marketing category
- ANDA
- Marketing start
- 2018-01-31
- 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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59726-505 | ALLERGY RELIEF (FEXOFENADINE HCL) TABLET, COATED [P & L DEVELOPMENT, LLC] | 5 | Legacy NDC | 20241103_3c178ebf-1bbc-4e2e-a123-447532c473d3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59726-505-15 | 59726050515 | 1 BOTTLE, PLASTIC in 1 BOX (59726-505-15) > 150 TABLET, COATED in 1 BOTTLE, PLASTIC | 2018-01-31 | 0000-00-00 | No | No | Current |
| 59726-505-30 | 59726050530 | 1 BOTTLE, PLASTIC in 1 BOX (59726-505-30) > 30 TABLET, COATED in 1 BOTTLE, PLASTIC | 2018-01-31 | 0000-00-00 | No | No | Current |