NDC 60512-6469

ALFALFA

Alfalfa

ALFALFA is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc.. The primary component is Alfalfa Whole.

• Product ID: 60512-6469_10c1ea72-3eaf-44b1-8639-4c1aded50551
• NDC: 60512-6469
• Product Type: Human Otc Drug
• Proprietary Name: ALFALFA
• Generic Name: Alfalfa
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1995-10-11
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: HOMEOLAB USA INC.
• Substance Name: ALFALFA WHOLE
• Active Ingredient Strength: 1 [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 60512-6469-1

80 PELLET in 1 TUBE (60512-6469-1)

• Marketing Start Date: 1995-10-11
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 60512-6469-1 [60512646901]

ALFALFA PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1995-10-11
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ALFALFA WHOLE	1 [hp_X]/1

OpenFDA Data

• SPL SET ID: 8b6756cf-46c2-4005-95cd-3ef657f4750d
• Manufacturer:
  • HOMEOLAB USA INC.

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