Allergy Relief
- Product NDC
- 68210-0450
- 11-digit product format
- 682100450
- Labeler code
- 68210
- Product ID
- 68210-0450_a0bf82fb-c556-a230-e053-2995a90a3b22
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Spirit Pharmaceutical LLC
- Application
- ANDA077829
- Marketing category
- ANDA
- Marketing start
- 2019-10-25
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 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 |
|---|
| 68210-0450-5 | 68210045005 | 1 BLISTER PACK in 1 CARTON (68210-0450-5) > 14 TABLET, FILM COATED in 1 BLISTER PACK | 1 blister pack | 2020-03-12 | 0000-00-00 | No | No | Current |