NDC 43547-290

bupropion

Bupropion Hydrochloride

bupropion is a Oral Tablet, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Solco Healthcare Us Llc. The primary component is Bupropion Hydrochloride.

• Product ID: 43547-290_1e71f995-cdb3-43e5-a181-1121c54df18d
• NDC: 43547-290
• Product Type: Human Prescription Drug
• Proprietary Name: bupropion
• Generic Name: Bupropion Hydrochloride
• Dosage Form: Tablet, Extended Release
• Route of Administration: ORAL
• Marketing Start Date: 2014-11-01
• Marketing Category: ANDA / ANDA
• Application Number: ANDA202304
• Labeler Name: Solco Healthcare US LLC
• Substance Name: BUPROPION HYDROCHLORIDE
• Active Ingredient Strength: 200 mg/1
• Pharm Classes: Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 43547-290-06

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (43547-290-06)

• Marketing Start Date: 2014-11-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43547-290-06 [43547029006]

bupropion TABLET, EXTENDED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA202304
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-11-01

NDC 43547-290-50 [43547029050]

bupropion TABLET, EXTENDED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA202304
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-11-01

NDC 43547-290-10 [43547029010]

bupropion TABLET, EXTENDED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA202304
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2014-11-01

NDC 43547-290-09 [43547029009]

bupropion TABLET, EXTENDED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA202304
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2014-11-01

Drug Details

Active Ingredients

Ingredient	Strength
BUPROPION HYDROCHLORIDE	200 mg/1

OpenFDA Data

• SPL SET ID: 39b2d509-1281-4464-9cf1-a94bbc18b84b
• Manufacturer:
  • Solco Healthcare US LLC
• UNII:
  • ZG7E5POY8O
• RxNorm Concept Unique ID - RxCUI:
  • 993518
  • 993536
  • 993503

Pharmacological Class

• Aminoketone [EPC]
• Dopamine Uptake Inhibitors [MoA]
• Increased Dopamine Activity [PE]
• Increased Norepinephrine Activity [PE]
• Norepinephrine Uptake Inhibitors [MoA]

Medicade Reported Pricing

43547029010 BUPROPION HCL SR 200 MG TABLET

Pricing Unit: EA | Drug Type:

43547029009 BUPROPION HCL SR 200 MG TABLET

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "bupropion" or generic name "Bupropion Hydrochloride"

NDC	Brand Name	Generic Name
68001-264	bupropion	bupropion
68382-353	bupropion	bupropion
68382-354	bupropion	bupropion
68788-7249	bupropion	bupropion
68788-9255	bupropion	bupropion
70518-1644	bupropion	bupropion
71335-0801	bupropion	bupropion
71335-0785	bupropion	bupropion
0615-8262	bupropion	bupropion
43547-288	bupropion	bupropion
43547-289	bupropion	bupropion
43547-290	bupropion	bupropion
50090-3854	bupropion	bupropion
50436-0289	bupropion	bupropion
55700-644	bupropion	bupropion
63187-521	bupropion	bupropion
65841-780	bupropion	bupropion
65841-836	bupropion	bupropion
70934-151	bupropion	bupropion
63629-8036	bupropion	bupropion
68788-7283	bupropion	bupropion
68071-5214	bupropion	bupropion
70518-2641	bupropion	bupropion
51655-357	bupropion	bupropion
71335-1622	bupropion	bupropion
0115-5445	Bupropion Hydrochloride	BUPROPION HYDROCHLORIDE
0115-6811	Bupropion Hydrochloride	BUPROPION HYDROCHLORIDE
0185-0410	Bupropion Hydrochloride	Bupropion Hydrochloride
0185-0415	Bupropion Hydrochloride	Bupropion Hydrochloride
0185-1111	Bupropion Hydrochloride	Bupropion Hydrochloride
0173-0135	WELLBUTRIN	bupropion hydrochloride
0173-0722	WELLBUTRIN	bupropion hydrochloride
0173-0947	WELLBUTRIN	bupropion hydrochloride
0173-0556	ZYBAN	bupropion hydrochloride