Pillstats
Rx only · Powder, For Suspension · Oral

Cefdinir

Cefdinir

10 ACTIVE SUPPLIERS — US
openFDA · updated weekly
US35 NDCs
10 active makers
UKComing
soon
CAComing
soon
AUComing
soon
EUComing
soon
RxCUI (US)25037
US makers10 labelers
Packages49
DEA / ScheduleNone

US acquisition costNADAC · per unit

Average across 16 priced NDCs. A benchmark of pharmacy acquisition cost — not a retail quote.

$0.035$0.071$0.106$0.142Dec 2025Apr 2026Jul 2026
$0.115
Latest avg · Jul 22, 2026
-7%
Since Dec 17, 2025
10
Active US suppliers
31%
Top-2 supplier share*

Medicaid dispensing volumeSDUD · per quarter

Prescriptions dispensed under Medicaid (fee-for-service + managed care), summed nationally. The closest free proxy to sales volume — Medicaid only, not all-payer.

258K517K775K1.0M2025 Q12025 Q22025 Q32025 Q42026 Q1
685K
Rx · 2026 Q1
54.4M
Units dispensed
-24%
Rx vs. year ago
5
Quarters · since 2025 Q1

Who makes it10 active · 0 exited

US labelers as registered with FDA. Repackagers relabel another company's product; share* is of listed packages, not sales.

LabelerTypePackagesStatus
Proficient Rx LPunknown8SUPPLYING
A-S Medication Solutionsunknown7SUPPLYING
NuCare Pharmaceuticals, Inc.unknown6SUPPLYING
Aurobindo Pharma Limitedunknown4SUPPLYING
Lupin Pharmaceuticals,Inc.unknown4SUPPLYING
Ascend Laboratories, LLCunknown4SUPPLYING
Direct_Rxunknown4SUPPLYING
Preferred Pharmaceuticals Inc.unknown4SUPPLYING
Teva Pharmaceuticals USA, Inc.unknown4SUPPLYING
Asclemed USA, Inc.unknown4SUPPLYING

Regulatory & supply eventsFDA · US

Shortages, recalls, and registration changes attached to this drug concept.

  • May 8, 2024
    RECALLRecall (Class II): Cefdinir for Oral Suspension USP, 250 mg/5 mL, packaged in a 60 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuti…

    Defective container: lack of seal integrity. — Recalling firm: Lupin Pharmaceuticals Inc. — USA Nationwide

  • Apr 24, 2024
    RECALLRecall (Class II): Cefdinir for Oral Suspension USP 250 mg/5 mL (60 mL when reconstituted), 60 mL bottle, Rx only, Manufactured for: Lupin…

    Presence of foreign substance: Product complaint of foreign material in reconstituted bottle. — Recalling firm: Lupin Pharmaceuticals Inc. — USA nationwide

  • Apr 24, 2024
    RECALLRecall (Class II): Cefdinir for Oral Suspension USP 125 mg/5 mL (60 mL when reconstituted), 60 mL bottle, Rx only, Manufactured for: Lupin…

    Presence of foreign substance: Product complaint of foreign material in reconstituted bottle. — Recalling firm: Lupin Pharmaceuticals Inc. — USA nationwide

  • Jul 2, 2020
    RECALLRecall (Class II): Cefdinir for Oral Suspension USP, 250 mg/5mL, packaged in 60 mL bottles, Rx only, Manufactured for: Lupin Pharmaceutica…

    Superpotent Drug: Out-of-specification (OOS) result observed in an assay test of retention samples. — Recalling firm: Lupin Pharmaceuticals Inc. — U.S.A. Nationwide

  • Nov 1, 2019
    RECALLRecall (Class III): Cefdinir for Oral Suspension USP, 250 mg/5mL,100 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Bal…

    Presence of Foreign substance: identified as a dead ant. — Recalling firm: Lupin Pharmaceuticals Inc. — Product was distributed to major distributors/wholesalers throughout the United States.

  • Nov 1, 2019
    RECALLRecall (Class III): Cefdinir for Oral Suspension USP, 125 mg/5mL, packaged in a) 60 mL bottle (NDC 68180-722-20), b) 100 mL bottle (NDC 681…

    Presence of Foreign substance: identified as a dead ant. — Recalling firm: Lupin Pharmaceuticals Inc. — Product was distributed to major distributors/wholesalers throughout the United States.

  • May 23, 2019
    RECALLRecall (Class II): Cefdinir for Oral Suspension USP, 250mg/5mL, Powder for oral suspension, 60 mL bottle, Rx only, Manufactured for: Lupin…

    Complaint received of metal piece identified in the product bottle prior to the reconstitution. — Recalling firm: Lupin Pharmaceuticals Inc. — Distributed Nationwide in the USA

  • Jan 2, 2019
    RECALLRecall (Class II): Cefdinir for Oral Suspension USP, 250mg/5mL, packaged in a) 60mL (NDC 68180-723-20), b)100mL (NDC 68180-723-10), Rx Onl…

    CGMP Deviations: Product complaints received indicating reconstituted suspension was observed to be thick. — Recalling firm: Lupin Pharmaceuticals Inc. — Nationwide within the United States

  • Jan 2, 2019
    RECALLRecall (Class II): Cefdinir for Oral Suspension USP, 125mg/5mL, packaged in a) 60mL (NDC 68180-722-20), b)100mL (NDC 68180-722-10), Rx Onl…

    CGMP Deviations: Product complaints received indicating reconstituted suspension was observed to be thick. — Recalling firm: Lupin Pharmaceuticals Inc. — Nationwide within the United States

  • Mar 27, 2018
    RECALLRecall (Class II): Lupin Cefdinir powder for Oral Suspension USP, 250 mg/5 mL in (a) 60 mL packs ( NDC 68180-723-20) and (b) 100 mL packs…

    Superpotent Drug — Recalling firm: Lupin Pharmaceuticals Inc. — Nationwide

  • Feb 26, 2013
    RECALLRecall (Class II): Cefdinir for Oral Suspension, 125 mg/5 mL, packaged in a) 60 mL bottle (NDC 0093-4136-64); b) 100 mL bottle (NDC 0093-4…

    Defective Container: This recall is being carried out due to the potential for improperly sealed bottles. — Recalling firm: Teva Pharmaceuticals USA, Inc. — Nationwide