acetaminophen

Generic: acetaminophen

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler camber pharmaceuticals, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

acetaminophen 10 mg/mL

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-205
Product ID 31722-205_e8c546a7-cc7c-a8de-e053-2995a90aad43
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216617
Listing Expiration 2026-12-31
Marketing Start 2022-07-27

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722205
Hyphenated Format 31722-205

Supplemental Identifiers

RxCUI
483017
UNII
362O9ITL9D

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 acetaminophen (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number ANDA216617 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 24 VIAL, SINGLE-DOSE in 1 CARTON (31722-205-24) / 100 mL in 1 VIAL, SINGLE-DOSE (31722-205-31)
source: ndc

Packages (1)

31722-205-24 24 VIAL, SINGLE-DOSE in 1 CARTON (31722-205-24) / 100 mL in 1 VIAL, SINGLE-DOSE (31722-205-31)

Ingredients (1)

acetaminophen (10 mg/mL)

Linked Drug Pages (1)

Acetaminophen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "e8c546a7-cc7c-a8de-e053-2995a90aad43", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["483017"], "spl_set_id": ["1c8fef8f-2ff5-4bea-bccb-90c2c8544c21"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 VIAL, SINGLE-DOSE in 1 CARTON (31722-205-24)  / 100 mL in 1 VIAL, SINGLE-DOSE (31722-205-31)", "package_ndc": "31722-205-24", "marketing_start_date": "20220727"}], "brand_name": "Acetaminophen", "product_id": "31722-205_e8c546a7-cc7c-a8de-e053-2995a90aad43", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "31722-205", "generic_name": "Acetaminophen", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "10 mg/mL"}], "application_number": "ANDA216617", "marketing_category": "ANDA", "marketing_start_date": "20220727", "listing_expiration_date": "20261231"}