50090-2219 : Amoxicillin and Clavulanate Potassium Oral Powder, for Suspension

NDC:	50090-2219
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Amoxicillin and Clavulanate Potassium
Dosage Form:	Oral Powder, for Suspension
Application #:	ANDA201091
Rev. Date:	Dec 20, 2011

NDC Package Codes:

50090-2219-0: 125 ML IN 1 BOTTLE (50090‑2219‑0)

Active Ingredients:

Amoxicillin
Clavulanate Potassium

Dosage Strength:

600 mg/5mL
42.9 mg/5mL

Pharmaceutical Classes:

Penicillin-class Antibacterial [EPC]
Penicillins [Chemical/Ingredient]
beta Lactamase Inhibitor [EPC]
beta Lactamase Inhibitors [MoA]

NDC QR Code

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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.