50090-2786 : Prednisone 20 mg Oral Tablet

NDC:	50090-2786
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Prednisone
Dosage Form:	Oral Tablet
Application #:	ANDA085161
Rev. Date:	Jan 1, 1990

NDC Package Codes:

50090-2786-0: 21 TABLET IN 1 BOTTLE (50090‑2786‑0)

Active Ingredients:

Prednisone

Dosage Strength:

20 mg

Pharmaceutical Classes:

Corticosteroid Hormone Receptor Agonists [MoA]
Corticosteroid [EPC]

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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.