Zyrtec Allergy
- Product NDC
- 52904-961
- 11-digit product format
- 529040961
- Labeler code
- 52904
- Product ID
- 52904-961_9c6b5944-6d45-4fd4-90c6-ac53a5590097
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- cetirizine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Select Corporation
- Application
- NDA019835
- Marketing category
- NDA
- Marketing start
- 2008-01-01
- 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52904-961-03 | Zyrtec Allergy | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 1 |
| 52904-961-03 | Zyrtec Allergy | 1 in 1 POUCH | TABLET, FILM COATED | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52904-961 | ZYRTEC ALLERGY (CETIRIZINE HYDROCHLORIDE) TABLET, FILM COATED [SELECT CORPORATION] | 1 | Legacy NDC, 2 package rows | 20220423_1ce1e74f-1f88-4cea-a19c-38748c151a02.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52904-961-03 | 52904096103 | 1 POUCH in 1 BLISTER PACK (52904-961-03) > 1 TABLET, FILM COATED in 1 POUCH | 1 pouch | 2008-01-01 | 0000-00-00 | No | No | Current |