methamphetamine hydrochloride

Generic: methamphetamine hydrochloride

Labeler: dr. reddy's laboratories inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methamphetamine hydrochloride
Generic Name methamphetamine hydrochloride
Labeler dr. reddy's laboratories inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methamphetamine hydrochloride 5 mg/1

Manufacturer
Dr. Reddy's Laboratories Inc

Identifiers & Regulatory

Product NDC 75907-094
Product ID 75907-094_c77198dd-fd98-ac84-9754-517e77c5c729
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091189
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2025-11-07

Pharmacologic Class

Classes
amphetamine anorectic [epc] amphetamines [cs] appetite suppression [pe] central nervous system stimulant [epc] central nervous system stimulation [pe] increased sympathetic activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 75907094
Hyphenated Format 75907-094

Supplemental Identifiers

RxCUI
977860
UPC
0375907094019
UNII
997F43Z9CV

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 methamphetamine hydrochloride (source: ndc)
Generic Name methamphetamine hydrochloride (source: ndc)
Application Number ANDA091189 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (75907-094-01)
source: ndc

Packages (1)

75907-094-01 100 TABLET in 1 BOTTLE, PLASTIC (75907-094-01)

Ingredients (1)

methamphetamine hydrochloride (5 mg/1)

Linked Drug Pages (1)

Methamphetamine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c77198dd-fd98-ac84-9754-517e77c5c729", "openfda": {"upc": ["0375907094019"], "unii": ["997F43Z9CV"], "rxcui": ["977860"], "spl_set_id": ["d0905e2c-a02f-ec4f-59a3-6f7ad0acbbf6"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (75907-094-01)", "package_ndc": "75907-094-01", "marketing_start_date": "20251107"}], "brand_name": "Methamphetamine Hydrochloride", "product_id": "75907-094_c77198dd-fd98-ac84-9754-517e77c5c729", "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": "75907-094", "dea_schedule": "CII", "generic_name": "METHAMPHETAMINE HYDROCHLORIDE", "labeler_name": "Dr. Reddy's Laboratories Inc", "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": "20251107", "listing_expiration_date": "20261231"}