NDC 50742-336 – Pramipexole dihydrochloride

Pramipexole Dihydrochloride 3.75 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC50742-336

Product details

Brand name
Pramipexole dihydrochloride
Generic name
Pramipexole dihydrochloride
Labeler
Ingenus Pharmaceuticals, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA213444
Marketed since
March 10, 2022
Listing expires
December 31, 2026
Pharmacologic class
Nonergot Dopamine Agonist

Active ingredients

Uses, dosage, side effects and warnings for Pramipexole dihydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
50742-336-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-336-30)Mar 10, 2022

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