NDC 62011-0071 – Loratadine and Pseudoephedrine Sulfate
Loratadine 10 mg/1; Pseudoephedrine Sulfate 240 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC62011-0071
Product details
- Brand name
- Loratadine and Pseudoephedrine Sulfate
- Generic name
- Loratadine and Pseudoephedrine Sulfate
- Labeler
- Strategic Sourcing Services LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA076557
- Marketed since
- June 6, 2017
- 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 |
|---|---|---|
| 62011-0071-1 | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (62011-0071-1) | Nov 17, 2004 |
| 62011-0071-2 | 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (62011-0071-2) | Jun 6, 2017 |
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