NDC 0220-0161

Alfalfa

Alfalfa

Alfalfa is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Boiron. The primary component is Alfalfa.

• Product ID: 0220-0161_83ea3411-ec59-d8de-e053-2991aa0a4bd5
• NDC: 0220-0161
• Product Type: Human Otc Drug
• Proprietary Name: Alfalfa
• Generic Name: Alfalfa
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Boiron
• Substance Name: ALFALFA
• Active Ingredient Strength: 6 [hp_C]/6[hp_C]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0220-0161-41

6 [hp_C] in 1 TUBE (0220-0161-41)

• Marketing Start Date: 1983-03-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0220-0161-41 [00220016141]

Alfalfa PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1983-03-03

Drug Details

Active Ingredients

Ingredient	Strength
ALFALFA	6 [hp_C]/6[hp_C]

OpenFDA Data

• SPL SET ID: 83ea3411-ec58-d8de-e053-2991aa0a4bd5
• Manufacturer:
  • Boiron
• UNII:
  • DJO934BRBD

NDC Crossover Matching brand name "Alfalfa" or generic name "Alfalfa"

NDC	Brand Name	Generic Name
0220-0161	Alfalfa	ALFALFA
0220-0164	Alfalfa	ALFALFA
15631-0014	ALFALFA	ALFALFA
15631-0507	ALFALFA	ALFALFA
22840-1507	Alfalfa	Medicago sativa
22840-1508	Alfalfa	Medicago sativa
22840-1509	Alfalfa	Medicago sativa
22840-1561	Alfalfa	Medicago sativa
22840-5503	Alfalfa	Medicago sativa
60512-6469	ALFALFA	ALFALFA
68428-872	Alfalfa	ALFALFA
71919-027	Alfalfa	ALFALFA
0268-1012	MEDICAGO SATIVA POLLEN	Alfalfa
0268-1013	MEDICAGO SATIVA POLLEN	Alfalfa
0268-6602	MEDICAGO SATIVA POLLEN	Alfalfa