NDC 21695-332

Albuterol Sulfate 2.5 mg per 3 mL solution

On the label: Rebel Distributors Corp... It's repackaged: Rebel Distributors Corp.. rebottles it from Nephron Pharmaceuticals Corporation's NDC 0487-9501.

Where the pills inside were made

Recalls

• Apr 13, 2022 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
  cGMP deviations: Temperature abuse
  Lots: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
• Apr 13, 2022 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
  cGMP deviations: Temperature abuse
  Lots: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
• Oct 2, 2013 · Class II · Nephron Pharmaceuticals Corp.
  Lack of Assurance of Sterility: Nephron Pharmaceuticals Corporation conducted a routine periodic aseptic process simulation and discovered bacterial growth in a number of media fill vials, exceeding the allowable limit.
  Lots: Lots #: A3A33A, A3A33B, A3A34A, A3A35A. A3A36A, A3A37A, A3A38A, Exp 06/15; A3A40A, A3A41A, A3A42A, Exp 07/15
• Jun 22, 2011 · Class II · Nephron Pharmaceuticals Corp.
  Lack of Assurance of Sterility
  Lots: Lot #: A0654A, Exp 07/12; A0A62A, Exp 10/12

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

Product details

Generic drug

Albuterol: every company that makes it

Form

solution

Strength

2.5 mg per 3 mL

Approval

ANDA ANDA074880

On the market since

Sep 17, 1997

Package NDCs

21695-332-25 21695-332-30

Official label

DailyMed (National Library of Medicine), updated Aug 31, 2010

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