NDC 51672-2085 – Childrens Loratadine
Loratadine 5 mg/5mL · Solution · Oral
Product NDC51672-2085
Product details
- Brand name
- Childrens Loratadine
- Generic name
- Loratadine
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Solution
- Route
- Oral
- Marketing category
- ANDA · ANDA076805
- Marketed since
- August 20, 2004
- Listing expires
- December 31, 2027
Active ingredients
- Loratadine 5 mg/5mL
Uses, dosage, side effects and warnings for Childrens Loratadine →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 51672-2085-1 | 1 BOTTLE in 1 CARTON (51672-2085-1) / 240 mL in 1 BOTTLE | Aug 20, 2004 |
| 51672-2085-4 | 1 BOTTLE in 1 CARTON (51672-2085-4) / 60 mL in 1 BOTTLE | Aug 20, 2004 |
| 51672-2085-5 | 1 BOTTLE in 1 CARTON (51672-2085-5) / 180 mL in 1 BOTTLE | Aug 20, 2004 |
| 51672-2085-8 | 1 BOTTLE in 1 CARTON (51672-2085-8) / 120 mL in 1 BOTTLE | Aug 20, 2004 |
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