Cetirizine Hydrochloride (Allergy)
- Product NDC
- 30142-169
- 11-digit product format
- 301420169
- Labeler code
- 30142
- Product ID
- 30142-169_185308e9-76a6-4245-bdab-06b22a79a400
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- KROGER COMPANY
- Application
- ANDA209107
- Marketing category
- ANDA
- Marketing start
- 2021-03-24
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 30142-169-12 | 30142016912 | 1 BOTTLE in 1 CARTON (30142-169-12) > 40 CAPSULE in 1 BOTTLE | 1 bottle | 2021-03-24 | 0000-00-00 | No | No | Current |
| 30142-169-53 | 30142016953 | 1 BOTTLE in 1 CARTON (30142-169-53) > 25 CAPSULE in 1 BOTTLE | 1 bottle | 2021-03-24 | 0000-00-00 | No | No | Current |