NDC 43742-0697

L Dopa

L-dopa

L Dopa is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Deseret Biologicals, Inc.. The primary component is Levodopa.

• Product ID: 43742-0697_e4ae37fa-9b9e-40d3-bc44-4fcfdf2ea209
• NDC: 43742-0697
• Product Type: Human Otc Drug
• Proprietary Name: L Dopa
• Generic Name: L-dopa
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2015-12-09
• Marketing End Date: 2023-06-06
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: LEVODOPA
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 43742-0697-1

30 mL in 1 BOTTLE, DROPPER (43742-0697-1)

• Marketing Start Date: 2015-12-09
• Marketing End Date: 2023-06-06
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0697-1 [43742069701]

L Dopa LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-12-09
• Marketing End Date: 2023-06-06

Drug Details

Active Ingredients

Ingredient	Strength
LEVODOPA	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: dc1ed9f0-2c71-4215-a560-b6a5bd3295b2
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • 46627O600J

NDC Crossover Matching brand name "L Dopa" or generic name "L-dopa"

NDC	Brand Name	Generic Name
43742-0027	L Dopa	L-Dopa
43742-0697	L Dopa	L-Dopa
43857-0265	L DOPA	not applicable
57520-0372	L Dopa Phenolic	L-dopa
43742-1307	L-Dopa	L-Dopa
43857-0226	L-Dopa	L-Dopa
63083-1514	L-Dopa	L-Dopa
44911-0035	L-Dopa Phenolic	L-Dopa