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NDC 55154-4152-00 Bupropion Hydrochloride 75 mg/1 Details
Bupropion Hydrochloride 75 mg/1
Bupropion Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Cardinal Health 107, LLC. The primary component is BUPROPION HYDROCHLORIDE.
Product Information
| NDC | 55154-4152 |
|---|---|
| Product ID | 55154-4152_ec4d2256-0340-4166-90ee-c264eef3ac82 |
| 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 | Bupropion Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Bupropion Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 75 |
| Active Ingredient Units | mg/1 |
| Substance Name | BUPROPION HYDROCHLORIDE |
| Labeler Name | Cardinal Health 107, LLC |
| Pharmaceutical Class | Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA076143 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 55154-4152-00 (55154415200)
| NDC Package Code | 55154-4152-0 |
|---|---|
| Billing NDC | 55154415200 |
| Package | 10 BLISTER PACK in 1 BAG (55154-4152-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK |
| Marketing Start Date | 2022-05-18 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |