50090-6189 : Gabapentin 800 mg Oral Tablet

NDC:	50090-6189
Labeler:	A-s Medication Solutions
Product Type:	Human Prescription Drug
Drug Name:	Gabapentin
Dosage Form:	Oral Tablet
Application #:	ANDA214957
Rev. Date:	Oct 1, 2021

NDC Package Codes:

50090-6189-0: 60 TABLET IN 1 BOTTLE (50090‑6189‑0)
50090-6189-1: 90 TABLET IN 1 BOTTLE (50090‑6189‑1)
50090-6189-2: 30 TABLET IN 1 BOTTLE (50090‑6189‑2)

Active Ingredients:

Gabapentin

Dosage Strength:

800 mg

Pharmaceutical Classes:

Anti-epileptic Agent [EPC]
Decreased Central Nervous System Disorganized Electrical Activity [PE]

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.