amantadine hydrochloride
Generic: amantadine hydrochloride
Labeler: st. mary's medical park pharmacyDrug Facts
Product Profile
Brand Name
amantadine hydrochloride
Generic Name
amantadine hydrochloride
Labeler
st. mary's medical park pharmacy
Dosage Form
CAPSULE
Routes
Active Ingredients
amantadine hydrochloride 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60760-779
Product ID
60760-779_3dd7e808-e0ec-8514-e063-6394a90a9f34
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212044
Listing Expiration
2026-12-31
Marketing Start
2020-05-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60760779
Hyphenated Format
60760-779
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
amantadine hydrochloride (source: ndc)
Generic Name
amantadine hydrochloride (source: ndc)
Application Number
ANDA212044 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE, PLASTIC (60760-779-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3dd7e808-e0ec-8514-e063-6394a90a9f34", "openfda": {"unii": ["M6Q1EO9TD0"], "rxcui": ["849389"], "spl_set_id": ["3dd7f2a6-5a91-81a2-e063-6294a90a33db"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (60760-779-30)", "package_ndc": "60760-779-30", "marketing_start_date": "20250826"}], "brand_name": "Amantadine Hydrochloride", "product_id": "60760-779_3dd7e808-e0ec-8514-e063-6394a90a9f34", "dosage_form": "CAPSULE", "pharm_class": ["Influenza A M2 Protein Inhibitor [EPC]", "M2 Protein Inhibitors [MoA]"], "product_ndc": "60760-779", "generic_name": "Amantadine Hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amantadine Hydrochloride", "active_ingredients": [{"name": "AMANTADINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA212044", "marketing_category": "ANDA", "marketing_start_date": "20200521", "listing_expiration_date": "20261231"}