all day allergy-D
- Product NDC
- 70677-0146
- 11-digit product format
- 706770146
- Labeler code
- 70677
- Product ID
- 70677-0146_694c3718-86b9-45ab-a49b-a4692b6e3fc9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Strategic Sourcing Services
- Application
- ANDA090922
- Marketing category
- ANDA
- Marketing start
- 2018-11-01
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
- Active strength
- 5 mg/1; mg/1
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70677-0146-1 | 70677014601 | 4 BLISTER PACK in 1 CARTON (70677-0146-1) > 6 TABLET in 1 BLISTER PACK | 4 blister pack | 2018-11-01 | 0000-00-00 | No | No | Current |