Allergy Relief
- Product NDC
- 69842-704
- 11-digit product format
- 698420704
- Labeler code
- 69842
- Product ID
- 69842-704_16c67165-aacb-4f32-b65b-949261ac97de
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine HCl
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- CVS Pharmacy
- Application
- ANDA079112
- Marketing category
- ANDA
- Marketing start
- 2017-10-31
- Marketing end
- 2025-05-30
- 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
- 0000-00-00
- 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 |
|---|
| 69842-704 | ALLERGY RELIEF (FEXOFENADINE HCL) TABLET, COATED [CVS PHARMACY] | 3 | Legacy NDC | 20221201_5b11cafe-f000-4e25-b2d0-a7297890b7f3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69842-704-70 | 69842070470 | 1 BOTTLE, PLASTIC in 1 BOX (69842-704-70) > 30 TABLET, COATED in 1 BOTTLE, PLASTIC | 2017-10-31 | 2025-05-30 | No | No | Current |