oxybutynin chloride

Generic: oxybutynin chloride

Labeler: ajanta pharma usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxybutynin chloride
Generic Name oxybutynin chloride
Labeler ajanta pharma usa inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

oxybutynin chloride 5 mg/1

Manufacturer
Ajanta Pharma USA Inc.

Identifiers & Regulatory

Product NDC 27241-155
Product ID 27241-155_7513158b-c4a4-4e1a-b329-55ee91c5569e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211655
Listing Expiration 2027-12-31
Marketing Start 2019-02-28

Pharmacologic Class

Classes
cholinergic muscarinic antagonist [epc] cholinergic muscarinic antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 27241155
Hyphenated Format 27241-155

Supplemental Identifiers

RxCUI
863619 863628 863636
UPC
0327241156045 0327241155048 0327241157042
UNII
L9F3D9RENQ

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 oxybutynin chloride (source: ndc)
Generic Name oxybutynin chloride (source: ndc)
Application Number ANDA211655 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-155-04)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-155-08)
source: ndc

Packages (2)

27241-155-04 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-155-04) 27241-155-08 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-155-08)

Ingredients (1)

oxybutynin chloride (5 mg/1)

Linked Drug Pages (1)

Oxybutynin Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7513158b-c4a4-4e1a-b329-55ee91c5569e", "openfda": {"upc": ["0327241156045", "0327241155048", "0327241157042"], "unii": ["L9F3D9RENQ"], "rxcui": ["863619", "863628", "863636"], "spl_set_id": ["95c2a144-ba0d-4011-ae0f-0e0ca876e8a8"], "manufacturer_name": ["Ajanta Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-155-04)", "package_ndc": "27241-155-04", "marketing_start_date": "20190228"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-155-08)", "package_ndc": "27241-155-08", "marketing_start_date": "20190228"}], "brand_name": "Oxybutynin Chloride", "product_id": "27241-155_7513158b-c4a4-4e1a-b329-55ee91c5569e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "27241-155", "generic_name": "Oxybutynin Chloride", "labeler_name": "Ajanta Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxybutynin Chloride", "active_ingredients": [{"name": "OXYBUTYNIN CHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA211655", "marketing_category": "ANDA", "marketing_start_date": "20190228", "listing_expiration_date": "20271231"}