acetaminophen for children

Generic: acetaminophen

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen for children
Generic Name acetaminophen
Labeler nucare pharmaceuticals,inc.
Dosage Form SUPPOSITORY
Routes
RECTAL
Active Ingredients

acetaminophen 120 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-4172
Product ID 68071-4172_1a3b93c2-3a06-fd40-e063-6394a90a6635
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA070607
Listing Expiration 2026-12-31
Marketing Start 2010-12-14

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680714172
Hyphenated Format 68071-4172

Supplemental Identifiers

RxCUI
198434
UPC
0368071417265
UNII
362O9ITL9D

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 acetaminophen for children (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number ANDA070607 (source: ndc)
Routes
RECTAL
source: ndc

Resolved Composition

Strengths
  • 120 mg/1
source: ndc
Packaging
  • 6 SUPPOSITORY in 1 BLISTER PACK (68071-4172-6)
source: ndc

Packages (1)

Ingredients (1)

acetaminophen (120 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["RECTAL"], "spl_id": "1a3b93c2-3a06-fd40-e063-6394a90a6635", "openfda": {"upc": ["0368071417265"], "unii": ["362O9ITL9D"], "rxcui": ["198434"], "spl_set_id": ["5f86e792-3262-4ee6-e053-2991aa0a54a0"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 SUPPOSITORY in 1 BLISTER PACK (68071-4172-6)", "package_ndc": "68071-4172-6", "marketing_start_date": "20171204"}], "brand_name": "acetaminophen for children", "product_id": "68071-4172_1a3b93c2-3a06-fd40-e063-6394a90a6635", "dosage_form": "SUPPOSITORY", "product_ndc": "68071-4172", "generic_name": "Acetaminophen", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "acetaminophen", "brand_name_suffix": "for children", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "120 mg/1"}], "application_number": "ANDA070607", "marketing_category": "ANDA", "marketing_start_date": "20101214", "listing_expiration_date": "20261231"}