FEXOFENADINE HYDROCHLORIDE
- Product NDC
- 68210-1220
- 11-digit product format
- 682101220
- Labeler code
- 68210
- Product ID
- 68210-1220_a0feb313-c93c-ba84-e053-2a95a90a9d1e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- FEXOFENADINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Spirit Pharmaceuticals LLC
- Application
- ANDA210137
- Marketing category
- ANDA
- Marketing start
- 2020-03-16
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 68210-1220-1 | 68210122001 | 1 BLISTER PACK in 1 BLISTER PACK (68210-1220-1) > 4 TABLET in 1 BLISTER PACK | 1 blister pack | 2020-03-16 | 0000-00-00 | No | No | Current |