Fexofenadine HCl and Pseudoephedrine HCI
- Product NDC
- 69842-249
- 11-digit product format
- 698420249
- Labeler code
- 69842
- Product ID
- 69842-249_e441b034-f450-a8e3-e9c0-9d93f884c742
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine HCl and Pseudoephedrine HCI
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- CVS Pharmacy
- Application
- ANDA076667
- Marketing category
- ANDA
- Marketing start
- 2019-07-19
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
- Active strength
- 60 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 69842-249 | FEXOFENADINE HCL AND PSEUDOEPHEDRINE HCI TABLET, EXTENDED RELEASE [CVS PHARMACY] | 16 | Legacy NDC | 20241030_d106f6b3-36df-e926-c298-b030dc79dbe6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69842-249-20 | 69842024920 | 4 BLISTER PACK in 1 CARTON (69842-249-20) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 4 blister pack | 2019-07-19 | 0000-00-00 | No | No | Current |
| 69842-249-30 | 69842024930 | 6 BLISTER PACK in 1 CARTON (69842-249-30) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 6 blister pack | 2019-07-19 | 0000-00-00 | No | No | Current |