Allergy Relief
- Product NDC
- 50066-310
- 11-digit product format
- 500660310
- Labeler code
- 50066
- Product ID
- 50066-310_bcf7a1d8-44eb-4883-9c9a-78e4837abbb3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl 10 mg
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Genomma Labs USA, Inc
- Application
- ANDA078317
- Marketing category
- ANDA
- Marketing start
- 2014-12-16
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50066-310-09 | 50066031009 | 1 BLISTER PACK in 1 CARTON (50066-310-09) > 10 TABLET in 1 BLISTER PACK | 1 blister pack | 2014-12-16 | 0000-00-00 | No | No | Current |
| 50066-310-45 | 50066031045 | 3 BLISTER PACK in 1 CARTON (50066-310-45) > 15 TABLET in 1 BLISTER PACK | 3 blister pack | 2014-12-16 | 0000-00-00 | No | No | Current |