NDC 73577-030

Belladonna and Opium

Atropa Belladonna And Opium

Belladonna and Opium is a Rectal Suppository in the Human Prescription Drug category. It is labeled and distributed by Legacy Pharma Inc.. The primary component is Atropa Belladonna; Opium.

• Product ID: 73577-030_5820d813-646c-4d00-9763-0747e3200e8e
• NDC: 73577-030
• Product Type: Human Prescription Drug
• Proprietary Name: Belladonna and Opium
• Generic Name: Atropa Belladonna And Opium
• Dosage Form: Suppository
• Route of Administration: RECTAL
• Marketing Start Date: 2020-04-29
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Legacy Pharma Inc.
• Substance Name: ATROPA BELLADONNA; OPIUM
• Active Ingredient Strength: 16 mg/1; mg/1
• DEA Schedule: CII
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 73577-030-12

12 PACKET in 1 CARTON (73577-030-12) > 1 SUPPOSITORY in 1 PACKET

• Marketing Start Date: 2020-04-29
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 73577-030-12 [73577003012]

Belladonna and Opium SUPPOSITORY

• Marketing Category: Unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2020-04-29

Drug Details

Active Ingredients

Ingredient	Strength
ATROPA BELLADONNA	16.2 mg/1

OpenFDA Data

• SPL SET ID: 28917da6-1cab-4f06-a1f4-c5bef5ecda13
• Manufacturer:
  • Legacy Pharma Inc.
• UNII:
  • WQZ3G9PF0H
  • 37M3MZ001L
• RxNorm Concept Unique ID - RxCUI:
  • 312104
  • 312107

NDC Crossover Matching brand name "Belladonna and Opium" or generic name "Atropa Belladonna And Opium"

NDC	Brand Name	Generic Name
0574-7040	Belladonna and Opium	ATROPA BELLADONNA and OPIUM
0574-7045	Belladonna and Opium	ATROPA BELLADONNA and OPIUM
63629-8435	Belladonna and Opium	ATROPA BELLADONNA and OPIUM
63629-8436	Belladonna and Opium	ATROPA BELLADONNA and OPIUM
73577-030	Belladonna and Opium	ATROPA BELLADONNA and OPIUM
73577-060	Belladonna and Opium	ATROPA BELLADONNA and OPIUM