NDC 27808-315 – Cabergoline

Cabergoline .5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC27808-315

Product details

Brand name
Cabergoline
Generic name
Cabergoline
Labeler
Cranbury Pharmaceuticals, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA220309
Marketed since
August 1, 2026
Listing expires
December 31, 2027
Pharmacologic class
Ergot Derivative

Active ingredients

Uses, dosage, side effects and warnings for Cabergoline →

Package NDC codes (1)

Package NDCDescriptionSince
27808-315-018 TABLET in 1 BOTTLE (27808-315-01)Aug 1, 2026

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