NDC 43742-0817

Acetylcholine Chloride

Acetylcholine Chloride

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

• Product ID: 43742-0817_fa2cfd77-dfe3-4a1e-985b-a2bfa45d4547
• NDC: 43742-0817
• Product Type: Human Otc Drug
• Proprietary Name: Acetylcholine Chloride
• Generic Name: Acetylcholine Chloride
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2016-07-21
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: ACETYLCHOLINE CHLORIDE
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 43742-0817-1

30 mL in 1 BOTTLE, DROPPER (43742-0817-1)

• Marketing Start Date: 2016-07-21
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0817-1 [43742081701]

Acetylcholine Chloride LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-07-21

Drug Details

Active Ingredients

Ingredient	Strength
ACETYLCHOLINE CHLORIDE	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 62fd8726-8be8-4d32-a11e-85c02ef368c8
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • AF73293C2R

NDC Crossover Matching brand name "Acetylcholine Chloride" or generic name "Acetylcholine Chloride"

NDC	Brand Name	Generic Name
43742-0164	Acetylcholine Chloride	Acetylcholine Chloride
43742-0817	Acetylcholine Chloride	Acetylcholine Chloride
43857-0138	Acetylcholine Chloride	Acetylcholine Chloride
43857-0270	Acetylcholine Chloride	Acetylcholine Chloride
63083-1502	Acetylcholine Chloride	Acetylcholine Chloride
24208-539	Miochol E	acetylcholine chloride