cevimeline hydrochloride
Generic: cevimeline hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
cevimeline hydrochloride
Generic Name
cevimeline hydrochloride
Labeler
bryant ranch prepack
Dosage Form
CAPSULE
Routes
Active Ingredients
cevimeline hydrochloride 30 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-2563
Product ID
72162-2563_fb360aef-a237-424f-95a0-f39d33113bd7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215056
Listing Expiration
2026-12-31
Marketing Start
2023-04-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721622563
Hyphenated Format
72162-2563
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
cevimeline hydrochloride (source: ndc)
Generic Name
cevimeline hydrochloride (source: ndc)
Application Number
ANDA215056 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (72162-2563-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fb360aef-a237-424f-95a0-f39d33113bd7", "openfda": {"unii": ["P81Q6V85NP"], "rxcui": ["309140"], "spl_set_id": ["71ada1b0-3344-4202-9277-57f1a37402c1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72162-2563-1)", "package_ndc": "72162-2563-1", "marketing_start_date": "20251104"}], "brand_name": "Cevimeline Hydrochloride", "product_id": "72162-2563_fb360aef-a237-424f-95a0-f39d33113bd7", "dosage_form": "CAPSULE", "pharm_class": ["Cholinergic Muscarinic Agonists [MoA]", "Cholinergic Receptor Agonist [EPC]"], "product_ndc": "72162-2563", "generic_name": "Cevimeline Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cevimeline Hydrochloride", "active_ingredients": [{"name": "CEVIMELINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA215056", "marketing_category": "ANDA", "marketing_start_date": "20230418", "listing_expiration_date": "20261231"}