NDC 54868-6224

Clonazepam 0.25 mg tablet, orally disintegrating

On the label: Physicians Total Care, Inc.. It's repackaged: Physicians Total Care, Inc. rebottles it from ENDO USA, Inc.'s NDC 49884-307.

Where the pills inside were made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants ENDO USA, Inc. names for other drugs.

Recalls

Nov 18, 2024 · Class I · Endo USA, Inc.
Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength.
Lots: Lot # 550176501, 550176601, Exp 02/28/2027.
Nov 18, 2024 · Class I · Endo USA, Inc.
Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength.
Lots: Lot #: 550174101, Exp. 01/31/2027.
Nov 18, 2024 · Class I · Endo USA, Inc.
Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength.
Lots: Lot #s: 550142801, 550142901, 550143001, 550143101, 550143201, 550143301, 550143401, 550147201, 550147401, Exp. 08/31/2026.
Nov 18, 2024 · Class I · Endo USA, Inc.
Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength.
Lots: Lot #s: 550145201, Exp. 08/31/2026; 550175901, 550176001, 550176201, Exp. 02/28/2027
Jul 10, 2024 · Class I · Endo Pharmaceuticals, Inc.
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.
Lots: Lot 550147301, Exp. 08/31/2026

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug: Clonazepam: every company that makes it
Form: tablet, orally disintegrating
Strength: 0.25 mg
Approval: ANDA ANDA077171
On the market since: Jan 14, 2011
Package NDCs: 49884-307-02 54868-6224-0
Official label: DailyMed (National Library of Medicine), updated Dec 1, 2010

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