NDC 63629-3762

Budeprion

Bupropion Hydrochloride

Budeprion is a Oral Tablet, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Bupropion Hydrochloride.

• Product ID: 63629-3762_45fa1a0a-5ee3-4cc2-b2cc-d7c12bed54a2
• NDC: 63629-3762
• Product Type: Human Prescription Drug
• Proprietary Name: Budeprion
• Generic Name: Bupropion Hydrochloride
• Dosage Form: Tablet, Extended Release
• Route of Administration: ORAL
• Marketing Start Date: 2008-05-30
• Marketing Category: ANDA / ANDA
• Application Number: ANDA077284
• Labeler Name: Bryant Ranch Prepack
• Substance Name: BUPROPION HYDROCHLORIDE
• Active Ingredient Strength: 150 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: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 63629-3762-2

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-3762-2)

• Marketing Start Date: 2008-05-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63629-3762-2 [63629376202]

Budeprion TABLET, EXTENDED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA077284
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2008-05-30
• Inactivation Date: 2019-11-27

NDC 63629-3762-4 [63629376204]

Budeprion TABLET, EXTENDED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA077284
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2008-05-30
• Inactivation Date: 2019-11-27

NDC 63629-3762-3 [63629376203]

Budeprion TABLET, EXTENDED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA077284
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2008-05-30
• Inactivation Date: 2019-11-27

NDC 63629-3762-1 [63629376201]

Budeprion TABLET, EXTENDED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA077284
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2008-05-30
• Inactivation Date: 2019-11-27

Drug Details

Active Ingredients

Ingredient	Strength
BUPROPION HYDROCHLORIDE	150 mg/1

OpenFDA Data

• SPL SET ID: 34743e9d-b87b-4158-8424-eaeb31ae85d5
• Manufacturer:
  • Bryant Ranch Prepack
• UNII:
  • ZG7E5POY8O

Pharmacological Class

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

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

NDC	Brand Name	Generic Name
63629-3762	Budeprion	Budeprion
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