phenobarbital

Generic: phenobarbital

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenobarbital
Generic Name phenobarbital
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phenobarbital 16.2 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-889
Product ID 71205-889_e8057c39-a5b1-491e-8dc5-2e697b17af38
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2019-05-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205889
Hyphenated Format 71205-889

Supplemental Identifiers

RxCUI
198086 199164 199167 199168
UPC
0371205893309 0371205891305 0371205889302 0371205892302
UNII
YQE403BP4D

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name phenobarbital (source: ndc)
Generic Name phenobarbital (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 16.2 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (71205-889-00)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (71205-889-11)
  • 30 TABLET in 1 BOTTLE, PLASTIC (71205-889-30)
  • 500 TABLET in 1 BOTTLE, PLASTIC (71205-889-55)
  • 60 TABLET in 1 BOTTLE, PLASTIC (71205-889-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (71205-889-90)
source: ndc

Packages (6)

71205-889-00 100 TABLET in 1 BOTTLE, PLASTIC (71205-889-00) 71205-889-11 1000 TABLET in 1 BOTTLE, PLASTIC (71205-889-11) 71205-889-30 30 TABLET in 1 BOTTLE, PLASTIC (71205-889-30) 71205-889-55 500 TABLET in 1 BOTTLE, PLASTIC (71205-889-55) 71205-889-60 60 TABLET in 1 BOTTLE, PLASTIC (71205-889-60) 71205-889-90 90 TABLET in 1 BOTTLE, PLASTIC (71205-889-90)

Ingredients (1)

phenobarbital (16.2 mg/1)

Linked Drug Pages (1)

Phenobarbital ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e8057c39-a5b1-491e-8dc5-2e697b17af38", "openfda": {"upc": ["0371205893309", "0371205891305", "0371205889302", "0371205892302"], "unii": ["YQE403BP4D"], "rxcui": ["198086", "199164", "199167", "199168"], "spl_set_id": ["71368966-b2d6-44cb-9418-050fe943af73"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (71205-889-00)", "package_ndc": "71205-889-00", "marketing_start_date": "20210803"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (71205-889-11)", "package_ndc": "71205-889-11", "marketing_start_date": "20210803"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (71205-889-30)", "package_ndc": "71205-889-30", "marketing_start_date": "20210803"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (71205-889-55)", "package_ndc": "71205-889-55", "marketing_start_date": "20210803"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (71205-889-60)", "package_ndc": "71205-889-60", "marketing_start_date": "20210803"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (71205-889-90)", "package_ndc": "71205-889-90", "marketing_start_date": "20210803"}], "brand_name": "Phenobarbital", "product_id": "71205-889_e8057c39-a5b1-491e-8dc5-2e697b17af38", "dosage_form": "TABLET", "product_ndc": "71205-889", "dea_schedule": "CIV", "generic_name": "Phenobarbital", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "16.2 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20190521", "listing_expiration_date": "20261231"}