phenobarbital oral solution

Generic: phenobarbital oral

Labeler: ajenat pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenobarbital oral solution
Generic Name phenobarbital oral
Labeler ajenat pharmaceuticals llc
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

phenobarbital 20 mg/5mL

Manufacturer
Ajenat Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 82983-417
Product ID 82983-417_92c0898e-5e8a-448e-8dfc-f944d12a637a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2025-11-05

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82983417
Hyphenated Format 82983-417

Supplemental Identifiers

RxCUI
702519
UPC
0382983417472
UNII
YQE403BP4D

Packaging Origin

Original Packager
true

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 oral solution (source: ndc)
Generic Name phenobarbital oral (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/5mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE, PLASTIC (82983-417-47)
source: ndc

Packages (1)

Ingredients (1)

phenobarbital (20 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "92c0898e-5e8a-448e-8dfc-f944d12a637a", "openfda": {"upc": ["0382983417472"], "unii": ["YQE403BP4D"], "rxcui": ["702519"], "spl_set_id": ["adf9382d-9fa3-4574-bfcd-e92a8b3433e6"], "manufacturer_name": ["Ajenat Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (82983-417-47)", "package_ndc": "82983-417-47", "marketing_start_date": "20251105"}], "brand_name": "Phenobarbital Oral Solution", "product_id": "82983-417_92c0898e-5e8a-448e-8dfc-f944d12a637a", "dosage_form": "SOLUTION", "product_ndc": "82983-417", "dea_schedule": "CIV", "generic_name": "Phenobarbital Oral", "labeler_name": "Ajenat Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital Oral Solution", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "20 mg/5mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20251105", "listing_expiration_date": "20261231"}