All Day Allergy
- Product NDC
- 59726-220
- 11-digit product format
- 597260220
- Labeler code
- 59726
- Product ID
- 59726-220_eb44a8b3-be84-4e0f-8e4a-14b928b347c8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- P and L Development of New York Corporation
- Application
- ANDA078427
- Marketing category
- ANDA
- Marketing start
- 2012-12-05
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59726-220 | ALL DAY ALLERGY ANTIHISTAMINE (CETIRIZINE HCL) TABLET [P AND L DEVELOPMENT OF NEW YORK CORPORATION] | 1 | Legacy NDC | 20121220_43e2621d-624f-4249-be54-e093367dab01.zip |