Allergy Relief
- Product NDC
- 57344-192
- 11-digit product format
- 573440192
- Labeler code
- 57344
- Product ID
- 57344-192_d010efeb-5f98-3620-e053-2995a90ad8ff
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AAA Pharmaceutical, Inc.
- Application
- ANDA204507
- Marketing category
- ANDA
- Marketing start
- 2018-06-01
- Marketing end
- 2023-02-28
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 57344-192-02 | 57344019202 | 1 BLISTER PACK in 1 CARTON (57344-192-02) > 5 TABLET in 1 BLISTER PACK | 1 blister pack | 2018-10-01 | 0000-00-00 | No | No | Current |
| 57344-192-04 | 57344019204 | 1 BOTTLE, PLASTIC in 1 CARTON (57344-192-04) > 30 TABLET in 1 BOTTLE, PLASTIC | | 2018-06-01 | 0000-00-00 | No | No | Current |
| 57344-192-06 | 57344019206 | 1 BOTTLE, PLASTIC in 1 CARTON (57344-192-06) > 45 TABLET in 1 BOTTLE, PLASTIC | | 2018-06-01 | 0000-00-00 | No | No | Current |