NDC 16571-667 – Phenobarbital

Phenobarbital 64.8 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC16571-667

Product details

Brand name
Phenobarbital
Generic name
Phenobarbital
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
UNAPPROVED DRUG OTHER
Marketed since
November 1, 2020
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Phenobarbital →

Package NDC codes (3)

Package NDCDescriptionSince
16571-667-01100 TABLET in 1 BOTTLE (16571-667-01)Nov 1, 2020
16571-667-101000 TABLET in 1 BOTTLE (16571-667-10)Nov 1, 2020
16571-667-50500 TABLET in 1 BOTTLE (16571-667-50)Nov 1, 2020

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