NDC 0065-0023

MIOSTAT

Carbachol

MIOSTAT is a Ophthalmic Solution in the Human Prescription Drug category. It is labeled and distributed by Alcon Laboratories, Inc.. The primary component is Carbachol.

• Product ID: 0065-0023_3cab3346-2363-4a2d-809a-933a00f26114
• NDC: 0065-0023
• Product Type: Human Prescription Drug
• Proprietary Name: MIOSTAT
• Generic Name: Carbachol
• Dosage Form: Solution
• Route of Administration: OPHTHALMIC
• Marketing Start Date: 1974-04-15
• Marketing Category: NDA / NDA
• Application Number: NDA016968
• Labeler Name: Alcon Laboratories, Inc.
• Substance Name: CARBACHOL
• Active Ingredient Strength: 0 mg/mL
• Pharm Classes: Cholinergic Agonists [MoA],Cholinergic Receptor Agonist [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 0065-0023-15

12 VIAL, GLASS in 1 CARTON (0065-0023-15) > 1.5 mL in 1 VIAL, GLASS

• Marketing Start Date: 1974-04-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0065-0023-15 [00065002315]

MIOSTAT SOLUTION

• Marketing Category: NDA
• Application Number: NDA016968
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 1974-04-15

Drug Details

Active Ingredients

Ingredient	Strength
CARBACHOL	.1 mg/mL

OpenFDA Data

• SPL SET ID: f28d7a56-e079-4a8b-ad81-9a97c780de67
• Manufacturer:
  • Alcon Laboratories, Inc.
• UNII:
  • 8Y164V895Y
• RxNorm Concept Unique ID - RxCUI:
  • 308966
  • 991606

Pharmacological Class

• Cholinergic Agonists [MoA]
• Cholinergic Receptor Agonist [EPC]