Allergy Relief
- Product NDC
- 50594-504
- 11-digit product format
- 505940504
- Labeler code
- 50594
- Product ID
- 50594-504_90469578-13e1-4c78-8d02-424573d6cc11
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine HCl
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Big Lots
- Application
- ANDA204507
- Marketing category
- ANDA
- Marketing start
- 2021-04-30
- 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 |
|---|
| 50594-504 | ALLERGY RELIEF (FEXOFENADINE HCL) TABLET, COATED [BIG LOTS] | 4 | Legacy NDC | 20241204_f43a08ec-e670-4043-af6e-60d3e0aadd59.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50594-504-30 | 50594050430 | 1 BOTTLE, PLASTIC in 1 BOX (50594-504-30) > 30 TABLET, COATED in 1 BOTTLE, PLASTIC | 2021-04-30 | 0000-00-00 | No | No | Current |