NDC 0363-0725 – Loratadine and Pseudoephedrine
Loratadine 10 mg/1; Pseudoephedrine Sulfate 240 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC0363-0725
Product details
- Brand name
- Loratadine and Pseudoephedrine
- Generic name
- Loratadine and Pseudoephedrine
- Labeler
- Walgreen Company
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA076557
- Marketed since
- November 7, 2013
- Listing expires
- December 31, 2026
- Pharmacologic class
- alpha-Adrenergic Agonist
Active ingredients
- Loratadine 10 mg/1
- Pseudoephedrine Sulfate 240 mg/1
Uses, dosage, side effects and warnings for Loratadine and Pseudoephedrine →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 0363-0725-15 | 1 BLISTER PACK in 1 CARTON (0363-0725-15) / 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Nov 7, 2013 |
| 0363-0725-56 | 1 BLISTER PACK in 1 CARTON (0363-0725-56) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Nov 7, 2013 |
| 0363-0725-69 | 1 BLISTER PACK in 1 CARTON (0363-0725-69) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Nov 7, 2013 |
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