Cetirizine Hydrochloride
- Product NDC
- 55700-331
- 11-digit product format
- 557000331
- Labeler code
- 55700
- Product ID
- 55700-331_72ed3b32-d2fb-44bc-af1f-f610db82ef45
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA077829
- Marketing category
- ANDA
- Marketing start
- 2009-10-01
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 55700-331-30 | 55700033130 | 30 TABLET in 1 BOTTLE (55700-331-30) | 30 tablet | 2015-07-24 | 0000-00-00 | No | No | Current |