amphetamine

Generic: amphetamine

Labeler: teva pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amphetamine
Generic Name amphetamine
Labeler teva pharmaceuticals, inc.
Dosage Form TABLET, ORALLY DISINTEGRATING
Routes
ORAL
Active Ingredients

amphetamine 18.8 mg/1

Manufacturer
Teva Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 0480-3320
Product ID 0480-3320_4373ba4a-1fee-46df-bba9-b60e42cfd15a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209253
DEA Schedule cii
Listing Expiration 2027-12-31
Marketing Start 2025-12-08

Pharmacologic Class

Established (EPC)
central nervous system stimulant [epc]
Physiologic Effect
central nervous system stimulation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04803320
Hyphenated Format 0480-3320

Supplemental Identifiers

RxCUI
1739803 1739813 1739819 1739825 1739831 1739837
UNII
CK833KGX7E
NUI
N0000175739 N0000175729

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 amphetamine (source: ndc)
Generic Name amphetamine (source: ndc)
Application Number ANDA209253 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 18.8 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (0480-3320-65) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
source: ndc

Packages (1)

0480-3320-65 30 BLISTER PACK in 1 CARTON (0480-3320-65) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

Ingredients (1)

amphetamine (18.8 mg/1)

Linked Drug Pages (1)

Amphetamine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4373ba4a-1fee-46df-bba9-b60e42cfd15a", "openfda": {"nui": ["N0000175739", "N0000175729"], "unii": ["CK833KGX7E"], "rxcui": ["1739803", "1739813", "1739819", "1739825", "1739831", "1739837"], "spl_set_id": ["243e88e7-6621-47e9-8d5c-3f79bcb088bb"], "pharm_class_pe": ["Central Nervous System Stimulation [PE]"], "pharm_class_epc": ["Central Nervous System Stimulant [EPC]"], "manufacturer_name": ["Teva Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0480-3320-65)  / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "0480-3320-65", "marketing_start_date": "20251208"}], "brand_name": "Amphetamine", "product_id": "0480-3320_4373ba4a-1fee-46df-bba9-b60e42cfd15a", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "0480-3320", "dea_schedule": "CII", "generic_name": "Amphetamine", "labeler_name": "Teva Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amphetamine", "active_ingredients": [{"name": "AMPHETAMINE", "strength": "18.8 mg/1"}], "application_number": "ANDA209253", "marketing_category": "ANDA", "marketing_start_date": "20251208", "listing_expiration_date": "20271231"}