0143-9982 : Amoxicillin and Clavulanate Potassium Oral Powder, for Suspension

NDC:	0143-9982
Labeler:	West-ward Pharmaceutical Corp
Product Type:	Human Prescription Drug
Drug Name:	Amoxicillin and Clavulanate Potassium
Dosage Form:	Oral Powder, for Suspension
Application #:	ANDA065191
Rev. Date:	Dec 1, 2007

NDC Package Codes:

0143-9982-01: 100 ML IN 1 BOTTLE (0143‑9982‑01)
0143-9982-50: 50 ML IN 1 BOTTLE (0143‑9982‑50)
0143-9982-75: 75 ML IN 1 BOTTLE (0143‑9982‑75)

Active Ingredients:

Amoxicillin
Clavulanic Acid

Dosage Strength:

400 mg/5mL
57 mg/5mL

Pharmaceutical Classes:

Penicillin-class Antibacterial [EPC]
Penicillins [CS]
beta Lactamase Inhibitor [EPC]
beta Lactamase Inhibitors [MoA]

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.