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NDC 55466-0132-12 Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, Amphetamine Sulfate 20; 20; 20; 20 mg/1; mg/1; mg/1; mg/1 Details
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, Amphetamine Sulfate 20; 20; 20; 20 mg/1; mg/1; mg/1; mg/1
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, Amphetamine Sulfate is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Neolpharma, Inc.. The primary component is AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE.
Product Information
NDC | 55466-0132 |
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Product ID | 55466-132_06445910-ddca-2206-e063-6394a90aa519 |
Associated GPIs | |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, Amphetamine Sulfate |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, Amphetamine Sulfate |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET |
Route | ORAL |
Active Ingredient Strength | 20; 20; 20; 20 |
Active Ingredient Units | mg/1; mg/1; mg/1; mg/1 |
Substance Name | AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE |
Labeler Name | Neolpharma, Inc. |
Pharmaceutical Class | Central Nervous System Stimulant [EPC], Central Nervous System Stimulant [EPC], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Central Nervous System Stimulation [PE], Central Nervous System Stimulation [PE] |
DEA Schedule | CII |
Marketing Category | ANDA |
Application Number | ANDA210754 |
Listing Certified Through | 2024-12-31 |
Package
NDC 55466-0132-12 (55466013212)
NDC Package Code | 55466-132-12 |
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Billing NDC | 55466013212 |
Package | 100 TABLET in 1 BOTTLE (55466-132-12) |
Marketing Start Date | 2023-12-29 |
NDC Exclude Flag | N |
Pricing Information | N/A |