NDC 51660-724 – Loratadine and Pseudoephedrine
Loratadine 10 mg/1; Pseudoephedrine Sulfate 240 mg/1 · Tablet, Extended Release · Oral
Product NDC51660-724
Product details
- Brand name
- Loratadine and Pseudoephedrine
- Generic name
- Loratadine and pseudoephedrine
- Labeler
- Ohm Laboratories Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA076557
- Marketed since
- November 17, 2004
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 51660-724-04 | 3 BLISTER PACK in 1 CARTON (51660-724-04) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Nov 17, 2004 |
| 51660-724-15 | 1 BLISTER PACK in 1 CARTON (51660-724-15) / 15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Nov 17, 2004 |
| 51660-724-69 | 1 BLISTER PACK in 1 CARTON (51660-724-69) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Nov 17, 2004 |
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