Allergy Relief
- Product NDC
- 50594-801
- 11-digit product format
- 505940801
- Labeler code
- 50594
- Product ID
- 50594-801_660bb090-3384-430c-a397-f5b34b245635
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine HCl
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Big Lots
- Application
- ANDA204507
- Marketing category
- ANDA
- Marketing start
- 2021-08-20
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50594-801 | ALLERGY RELIEF (FEXOFENADINE HCL) TABLET, COATED [BIG LOTS] | 4 | Legacy NDC | 20221012_3a445198-4dd1-4b8a-bf86-3518b00a8b3b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50594-801-30 | 50594080130 | 1 BOTTLE, PLASTIC in 1 BOX (50594-801-30) > 30 TABLET, COATED in 1 BOTTLE, PLASTIC | 2021-08-20 | 0000-00-00 | No | No | Current |