Cefdinir 250 mg per 5 mL powder, for suspension

Where it's 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 Teva Pharmaceuticals USA, Inc. names for other drugs.

Recalls

• Feb 26, 2013 · Class II · Teva Pharmaceuticals USA, Inc.
  Defective Container: This recall is being carried out due to the potential for improperly sealed bottles.
  Lots: a) Lot #: 30304253A, Exp 12/13; b) Lot #: 30304144A, Exp 12/13 and 30304477A, Exp 03/14

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

Product details

Generic drug

Cefdinir: every company that makes it

Form

powder, for suspension, oral

Strength

250 mg per 5 mL

Approval

ANDA ANDA065332

On the market since

May 8, 2007

Package NDCs

0093-4137-64 0093-4137-73

Official label

DailyMed (National Library of Medicine), updated Feb 1, 2023

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?