gesteira
Generic: acetaminophen
Labeler: menper distributors, inc.Drug Facts
Product Profile
Brand Name
gesteira
Generic Name
acetaminophen
Labeler
menper distributors, inc.
Dosage Form
LIQUID
Routes
Active Ingredients
acetaminophen 675 mg/15mL
Manufacturer
Identifiers & Regulatory
Product NDC
53145-052
Product ID
53145-052_3a89ea39-3fbe-7bc0-e063-6294a90aed2d
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2012-02-21
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
53145052
Hyphenated Format
53145-052
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
gesteira (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 675 mg/15mL
Packaging
- 1 BOTTLE in 1 CARTON (53145-052-04) / 120 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a89ea39-3fbe-7bc0-e063-6294a90aed2d", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["2719840"], "spl_set_id": ["5a907289-564c-491b-98d5-d7f43eaaa1b2"], "manufacturer_name": ["Menper Distributors, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (53145-052-04) / 120 mL in 1 BOTTLE", "package_ndc": "53145-052-04", "marketing_start_date": "20120221"}], "brand_name": "Gesteira", "product_id": "53145-052_3a89ea39-3fbe-7bc0-e063-6294a90aed2d", "dosage_form": "LIQUID", "product_ndc": "53145-052", "generic_name": "Acetaminophen", "labeler_name": "Menper Distributors, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Gesteira", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "675 mg/15mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120221", "listing_expiration_date": "20261231"}