NDC 68180-153 – Desloratadine
Desloratadine 5 mg/1 · Tablet, Film Coated · Oral
Product NDC68180-153
Product details
- Brand name
- Desloratadine
- Generic name
- Desloratadine
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078352
- Marketed since
- February 25, 2013
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Desloratadine 5 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68180-153-01 | 100 TABLET, FILM COATED in 1 BOTTLE (68180-153-01) | Feb 25, 2013 |
| 68180-153-02 | 500 TABLET, FILM COATED in 1 BOTTLE (68180-153-02) | Feb 25, 2013 |
Recalls mentioning this NDC
- D-0221-2024 Jan 17, 2024 · Class II
CGMP Deviations: N-Nitroso Desloratadine impurity result exceeded the acceptable intake limit.
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