Cetirizine Hydrochloride (Allergy)
- Product NDC
- 10202-715
- 11-digit product format
- 102020715
- Labeler code
- 10202
- Product ID
- 10202-715_cfc3ae79-c9c9-4ad2-a2a2-bbce5b288a1e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- 7-Eleven
- Application
- ANDA090760
- Marketing category
- ANDA
- Marketing start
- 2020-02-04
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 10202-715-01 | 10202071501 | 1 BLISTER PACK in 1 CARTON (10202-715-01) > 14 TABLET in 1 BLISTER PACK | 1 blister pack | 2020-02-04 | 0000-00-00 | No | No | Current |