NDC 24208-539

Miochol E

Acetylcholine Chloride

Miochol E is a Kit in the Human Prescription Drug category. It is labeled and distributed by Bausch & Lomb Incorporated. The primary component is .

• Product ID: 24208-539_3ab8a525-6c7e-406d-90ec-85cc820d0f62
• NDC: 24208-539
• Product Type: Human Prescription Drug
• Proprietary Name: Miochol E
• Generic Name: Acetylcholine Chloride
• Dosage Form: Kit
• Marketing Start Date: 1993-09-22
• Marketing Category: NDA / NDA
• Application Number: NDA020213
• Labeler Name: Bausch & Lomb Incorporated
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2024-12-31

Packaging

NDC 24208-539-20

1 KIT in 1 BLISTER PACK (24208-539-20) * 2 mL in 1 VIAL * 2 mL in 1 AMPULE

• Marketing Start Date: 1993-09-22
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 24208-539-20 [24208053920]

Miochol E KIT

• Marketing Category: NDA
• Application Number: NDA020213
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1993-09-22

Drug Details

OpenFDA Data

• SPL SET ID: e701ef07-9499-4b56-931f-f4eb3eedbe24
• Manufacturer:
  • Bausch & Lomb Incorporated
• RxNorm Concept Unique ID - RxCUI:
  • 876551
  • 876553

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

NDC	Brand Name	Generic Name
24208-539	Miochol E	acetylcholine chloride
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