phenobarbital

Generic: phenobarbital

Labeler: pharmaceutical associates, inc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenobarbital
Generic Name phenobarbital
Labeler pharmaceutical associates, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

phenobarbital 20 mg/5mL

Manufacturer
Pharmaceutical Associates, Inc.

Identifiers & Regulatory

Product NDC 0121-0531
Product ID 0121-0531_d4dbd9ed-e7bc-038e-e053-2a95a90a8a27
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2007-02-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01210531
Hyphenated Format 0121-0531

Supplemental Identifiers

RxCUI
702519
UPC
0301210531163
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 (source: ndc)
Generic Name phenobarbital (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/5mL
source: ndc
Packaging
  • 10 TRAY in 1 CASE (0121-0531-05) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE
  • 10 TRAY in 1 CASE (0121-0531-07) / 10 CUP, UNIT-DOSE in 1 TRAY / 7.5 mL in 1 CUP, UNIT-DOSE
  • 10 TRAY in 1 CASE (0121-0531-15) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE
  • 12 BOTTLE in 1 CASE (0121-0531-16) / 473 mL in 1 BOTTLE
source: ndc

Packages (4)

Ingredients (1)

phenobarbital (20 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d4dbd9ed-e7bc-038e-e053-2a95a90a8a27", "openfda": {"upc": ["0301210531163"], "unii": ["YQE403BP4D"], "rxcui": ["702519"], "spl_set_id": ["037c7532-7688-44fd-8c76-d25e8adf5fb5"], "manufacturer_name": ["Pharmaceutical Associates, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TRAY in 1 CASE (0121-0531-05)  / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE", "package_ndc": "0121-0531-05", "marketing_start_date": "20070219"}, {"sample": false, "description": "10 TRAY in 1 CASE (0121-0531-07)  / 10 CUP, UNIT-DOSE in 1 TRAY / 7.5 mL in 1 CUP, UNIT-DOSE", "package_ndc": "0121-0531-07", "marketing_start_date": "20070219"}, {"sample": false, "description": "10 TRAY in 1 CASE (0121-0531-15)  / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE", "package_ndc": "0121-0531-15", "marketing_start_date": "20070219"}, {"sample": false, "description": "12 BOTTLE in 1 CASE (0121-0531-16)  / 473 mL in 1 BOTTLE", "package_ndc": "0121-0531-16", "marketing_start_date": "20070219"}], "brand_name": "Phenobarbital", "product_id": "0121-0531_d4dbd9ed-e7bc-038e-e053-2a95a90a8a27", "dosage_form": "SOLUTION", "product_ndc": "0121-0531", "dea_schedule": "CIV", "generic_name": "Phenobarbital", "labeler_name": "Pharmaceutical Associates, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "20 mg/5mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20070219", "listing_expiration_date": "20261231"}