Allergy
- Product NDC
- 10202-107
- 11-digit product format
- 102020107
- Labeler code
- 10202
- Product ID
- 10202-107_8a212704-7ca1-4169-ef4d-56d85b24dc0e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- 7-Eleven
- Application
- ANDA076502
- Marketing category
- ANDA
- Marketing start
- 2019-11-15
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10202-107 | ALLERGY (FEXOFENADINE HYDROCHLORIDE) TABLET [7-ELEVEN] | 3 | Legacy NDC | 20241101_7031766f-cf19-8bea-89e5-1342d1dc29eb.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 10202-107-10 | 10202010710 | 2 BLISTER PACK in 1 CARTON (10202-107-10) > 5 TABLET in 1 BLISTER PACK | 2 blister pack | 2019-11-15 | 0000-00-00 | No | No | Current |