phenobarbital

Generic: phenobarbital

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenobarbital
Generic Name phenobarbital
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

phenobarbital 32.4 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4129
Product ID 70518-4129_3fa56bec-cf88-ce76-e063-6294a90ae2bb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2024-07-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184129
Hyphenated Format 70518-4129

Supplemental Identifiers

RxCUI
199167
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
  • 32.4 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-4129-0)
source: ndc

Packages (1)

70518-4129-0 30 TABLET in 1 BLISTER PACK (70518-4129-0)

Ingredients (1)

phenobarbital (32.4 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": "3fa56bec-cf88-ce76-e063-6294a90ae2bb", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["199167"], "spl_set_id": ["4e2910f2-173d-4b5c-aad3-44f4ab40d8cb"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4129-0)", "package_ndc": "70518-4129-0", "marketing_start_date": "20240701"}], "brand_name": "Phenobarbital", "product_id": "70518-4129_3fa56bec-cf88-ce76-e063-6294a90ae2bb", "dosage_form": "TABLET", "product_ndc": "70518-4129", "dea_schedule": "CIV", "generic_name": "Phenobarbital", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "32.4 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20240701", "listing_expiration_date": "20261231"}