NDC 68788-9138 – Orphenadrine Citrate

Orphenadrine Citrate 100 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC68788-9138

Product details

Brand name
Orphenadrine Citrate
Generic name
Orphenadrine Citrate
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA040284
Marketed since
June 19, 1998
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Orphenadrine citrate →

Package NDC codes (7)

Package NDCDescriptionSince
68788-9138-1100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9138-1)Nov 22, 2011
68788-9138-220 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9138-2)Nov 22, 2011
68788-9138-330 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9138-3)Nov 22, 2011
68788-9138-414 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9138-4)Nov 22, 2011
68788-9138-660 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9138-6)Nov 22, 2011
68788-9138-8120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9138-8)Nov 22, 2011
68788-9138-990 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9138-9)Nov 22, 2011

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