oxybutynin chloride
Generic: oxybutynin chloride
Labeler: atlantic biologicals corp.Drug Facts
Product Profile
Brand Name
oxybutynin chloride
Generic Name
oxybutynin chloride
Labeler
atlantic biologicals corp.
Dosage Form
SYRUP
Routes
Active Ingredients
oxybutynin chloride 5 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
17856-0149
Product ID
17856-0149_35cef500-044f-9368-e063-6294a90a9ae5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA074520
Listing Expiration
2026-12-31
Marketing Start
1996-03-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
178560149
Hyphenated Format
17856-0149
Supplemental Identifiers
RxCUI
UNII
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
oxybutynin chloride (source: ndc)
Generic Name
oxybutynin chloride (source: ndc)
Application Number
ANDA074520 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/5mL
Packaging
- 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0149-1) / 5 mL in 1 CUP, UNIT-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "35cef500-044f-9368-e063-6294a90a9ae5", "openfda": {"unii": ["L9F3D9RENQ"], "rxcui": ["863599"], "spl_set_id": ["fe4ed76b-0009-455f-be30-47e80fc1afdf"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0149-1) / 5 mL in 1 CUP, UNIT-DOSE", "package_ndc": "17856-0149-1", "marketing_start_date": "20200305"}], "brand_name": "Oxybutynin Chloride", "product_id": "17856-0149_35cef500-044f-9368-e063-6294a90a9ae5", "dosage_form": "SYRUP", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "17856-0149", "generic_name": "Oxybutynin Chloride", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA074520", "marketing_category": "ANDA", "marketing_start_date": "19960329", "listing_expiration_date": "20261231"}