NDC 68788-7765 – Nabumetone

Nabumetone 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-7765

Product details

Brand name
Nabumetone
Generic name
Nabumetone
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078420
Marketed since
July 15, 2020
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Nabumetone →

Package NDC codes (6)

Package NDCDescriptionSince
68788-7765-1100 TABLET in 1 BOTTLE (68788-7765-1)Jul 15, 2020
68788-7765-220 TABLET in 1 BOTTLE (68788-7765-2)Jul 15, 2020
68788-7765-330 TABLET in 1 BOTTLE (68788-7765-3)Jul 15, 2020
68788-7765-660 TABLET in 1 BOTTLE (68788-7765-6)Jul 15, 2020
68788-7765-8120 TABLET in 1 BOTTLE (68788-7765-8)Jul 15, 2020
68788-7765-990 TABLET in 1 BOTTLE (68788-7765-9)Jul 15, 2020

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