NDC 0904-5833 – Loratadine and Pseudoephedrine Sulfate
Loratadine 10 mg/1; Pseudoephedrine Sulfate 240 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC0904-5833
Product details
- Brand name
- Loratadine and Pseudoephedrine Sulfate
- Generic name
- Loratadine and Pseudoephedrine Sulfate
- Labeler
- Major Pharmaceuticals
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA076557
- Marketed since
- November 17, 2004
- 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 Sulfate →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0904-5833-15 | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0904-5833-15) | Nov 17, 2004 |
| 0904-5833-48 | 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0904-5833-48) | Nov 17, 2004 |
Recalls mentioning this NDC
- D-0068-2022 Nov 3, 2021 · Class III
Failed Moisture Limits
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