methamphetamine hydrochloride
Generic: methamphetamine hydrochloride
Labeler: mayne pharma commercial llcDrug Facts
Product Profile
Brand Name
methamphetamine hydrochloride
Generic Name
methamphetamine hydrochloride
Labeler
mayne pharma commercial llc
Dosage Form
TABLET
Routes
Active Ingredients
methamphetamine hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68308-115
Product ID
68308-115_ffc2cd39-e42b-5821-e053-6394a90a9974
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091189
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
2010-04-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68308115
Hyphenated Format
68308-115
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
methamphetamine hydrochloride (source: ndc)
Generic Name
methamphetamine hydrochloride (source: ndc)
Application Number
ANDA091189 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 100 TABLET in 1 BOTTLE, PLASTIC (68308-115-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ffc2cd39-e42b-5821-e053-6394a90a9974", "openfda": {"unii": ["997F43Z9CV"], "rxcui": ["977860"], "spl_set_id": ["f31f580f-1f08-4a0f-b078-0b9e3308f712"], "manufacturer_name": ["Mayne Pharma Commercial LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (68308-115-01)", "package_ndc": "68308-115-01", "marketing_start_date": "20100426"}], "brand_name": "Methamphetamine Hydrochloride", "product_id": "68308-115_ffc2cd39-e42b-5821-e053-6394a90a9974", "dosage_form": "TABLET", "pharm_class": ["Amphetamine Anorectic [EPC]", "Amphetamines [CS]", "Appetite Suppression [PE]", "Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]", "Increased Sympathetic Activity [PE]"], "product_ndc": "68308-115", "dea_schedule": "CII", "generic_name": "METHAMPHETAMINE HYDROCHLORIDE", "labeler_name": "Mayne Pharma Commercial LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methamphetamine Hydrochloride", "active_ingredients": [{"name": "METHAMPHETAMINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA091189", "marketing_category": "ANDA", "marketing_start_date": "20100426", "listing_expiration_date": "20261231"}