71610-621 : Gabapentin 600 mg Oral Tablet

NDC:	71610-621
Labeler:	Aphena Pharma Solutions - Tennessee, LLC
Product Type:	Human Prescription Drug
Drug Name:	Gabapentin
Dosage Form:	Oral Tablet
Application #:	ANDA214957
Rev. Date:	Oct 1, 2021

NDC Package Codes:

71610-621-15: 15 TABLET IN 1 BOTTLE (71610‑621‑15)
71610-621-30: 30 TABLET IN 1 BOTTLE (71610‑621‑30)
71610-621-45: 45 TABLET IN 1 BOTTLE (71610‑621‑45)
71610-621-53: 60 TABLET IN 1 BOTTLE (71610‑621‑53)
71610-621-60: 90 TABLET IN 1 BOTTLE (71610‑621‑60)
71610-621-70: 120 TABLET IN 1 BOTTLE (71610‑621‑70)
71610-621-73: 135 TABLET IN 1 BOTTLE (71610‑621‑73)
71610-621-80: 180 TABLET IN 1 BOTTLE (71610‑621‑80)
71610-621-92: 270 TABLET IN 1 BOTTLE (71610‑621‑92)
71610-621-94: 360 TABLET IN 1 BOTTLE (71610‑621‑94)

Active Ingredients:

Gabapentin

Dosage Strength:

600 mg

Pharmaceutical Classes:

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

NDC QR Code

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NDC 71610-621 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.