NDC 71205-889 – Phenobarbital

Phenobarbital 16.2 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71205-889

Product details

Brand name
Phenobarbital
Generic name
Phenobarbital
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
UNAPPROVED DRUG OTHER
Marketed since
May 21, 2019
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Phenobarbital →

Package NDC codes (6)

Package NDCDescriptionSince
71205-889-00100 TABLET in 1 BOTTLE, PLASTIC (71205-889-00)Aug 3, 2021
71205-889-111000 TABLET in 1 BOTTLE, PLASTIC (71205-889-11)Aug 3, 2021
71205-889-3030 TABLET in 1 BOTTLE, PLASTIC (71205-889-30)Aug 3, 2021
71205-889-55500 TABLET in 1 BOTTLE, PLASTIC (71205-889-55)Aug 3, 2021
71205-889-6060 TABLET in 1 BOTTLE, PLASTIC (71205-889-60)Aug 3, 2021
71205-889-9090 TABLET in 1 BOTTLE, PLASTIC (71205-889-90)Aug 3, 2021

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