NDC 49884-310 – Clonazepam
Clonazepam 2 mg/1 · Tablet, Orally Disintegrating · Oral
Product NDC49884-310
Product details
- Brand name
- Clonazepam
- Generic name
- clonazepam
- Labeler
- Par Health USA, LLC
- Dosage form
- Tablet, Orally Disintegrating
- Route
- Oral
- Marketing category
- ANDA · ANDA077171
- Marketed since
- August 5, 2005
- Listing expires
- December 31, 2027
- Pharmacologic class
- Benzodiazepine
Active ingredients
- Clonazepam 2 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 49884-310-02 | 60 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49884-310-02) | Aug 5, 2005 |
Recalls mentioning this NDC
- D-0180-2025 Jan 15, 2025 · Class I
Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength. - D-0178-2025 Jan 15, 2025 · Class I
Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength. - D-0179-2025 Jan 15, 2025 · Class I
Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength. - D-0181-2025 Jan 15, 2025 · Class I
Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength. - D-0622-2024 Aug 7, 2024 · Class I
Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled as 0.125 mg instead of 0.25 mg. The blister strips inside the product carton reflect the correct strength of 0.25 mg.
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