NDC 51672-5332 – Phenobarbital

Phenobarbital 30 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC51672-5332

Product details

Brand name
Phenobarbital
Generic name
Phenobarbital
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
UNAPPROVED DRUG OTHER
Marketed since
August 1, 2024
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Phenobarbital →

Package NDC codes (2)

Package NDCDescriptionSince
51672-5332-1100 TABLET in 1 BOTTLE, PLASTIC (51672-5332-1)Aug 1, 2024
51672-5332-31000 TABLET in 1 BOTTLE, PLASTIC (51672-5332-3)Aug 1, 2024

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