Zero Allergy
- Product NDC
- 58593-827
- 11-digit product format
- 585930827
- Labeler code
- 58593
- Product ID
- 58593-827_fe73cafa-ccf5-4659-9fc3-485825958f51
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Efficient Laboratories Inc
- Application
- ANDA077498
- Marketing category
- ANDA
- Marketing start
- 2013-04-01
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 58593-827-14 | 58593082714 | 14 TABLET in 1 BLISTER PACK (58593-827-14) | 14 tablet | 2013-04-01 | 0000-00-00 | No | No | Current |