Cetirizine HCL 10 mg All Day Allergy Relief
- Product NDC
- 55315-129
- 11-digit product format
- 553150129
- Labeler code
- 55315
- Product ID
- 55315-129_c63e19f3-ecfa-45f5-bd6e-a67ff2c6ecb9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Freds Inc
- Application
- ANDA078780
- Marketing category
- ANDA
- Marketing start
- 2013-03-01
- Marketing end
- 2021-12-30
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 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 |
|---|
| 55315-129-30 | 55315012930 | 2 BLISTER PACK in 1 CARTON (55315-129-30) > 15 TABLET in 1 BLISTER PACK | 2 blister pack | 2013-03-01 | 2021-12-30 | No | No | Current |