all day allergy
- Product NDC
- 70677-0006
- 11-digit product format
- 706770006
- Labeler code
- 70677
- Product ID
- 70677-0006_e9e258a3-bfd3-4434-8055-02b9d733f7ca
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA090760
- Marketing category
- ANDA
- Marketing start
- 2015-08-05
- Marketing end
- 2020-06-30
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record