NDC 43742-0164

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: 43742-0164_01f7e666-929a-418f-a6e4-31226ed47bcc
• NDC: 43742-0164
• Product Type: Human Otc Drug
• Proprietary Name: Acetylcholine Chloride
• Generic Name: Acetylcholine Chloride
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2013-09-11
• Marketing End Date: 2021-02-10
• 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

Packaging

NDC 43742-0164-1

30 mL in 1 BOTTLE, DROPPER (43742-0164-1)

• Marketing Start Date: 2013-09-11
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0164-1 [43742016401]

Acetylcholine Chloride LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-09-11
• Marketing End Date: 2021-02-10

Drug Details

Active Ingredients

Ingredient	Strength
ACETYLCHOLINE CHLORIDE	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 2bc74ff2-09fb-4f4a-af90-4d6ce0256945
• 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