Cetirizine Hydrochloride
- Product NDC
- 70985-001
- 11-digit product format
- 709850001
- Labeler code
- 70985
- Product ID
- 70985-001_cfd290fe-1a76-c40c-e053-2995a90afb10
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Drug Ocean LLC
- Application
- ANDA077829
- Marketing category
- ANDA
- Marketing start
- 2016-11-08
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70985-001 | CETIRIZINE HYDROCHLORIDE TABLET [DRUG OCEAN LLC] | 5 | Legacy NDC | 20231224_da7b0ec8-fd3b-4b07-b196-edbc72a53b3f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70985-001-01 | 70985000101 | 100 TABLET in 1 BOTTLE (70985-001-01) | 100 tablet | 2016-11-08 | 0000-00-00 | No | No | Current |
| 70985-001-02 | 70985000102 | 500 TABLET in 1 BOTTLE (70985-001-02) | 500 tablet | 2016-11-08 | 0000-00-00 | No | No | Current |