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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 020213

MIOCHOL-E (ACETYLCHOLINE CHLORIDE)
20MG/VIAL
Marketing Status: Prescription
Active Ingredient: ACETYLCHOLINE CHLORIDE
Proprietary Name: MIOCHOL-E
Dosage Form; Route of Administration: FOR SOLUTION; OPHTHALMIC
Strength: 20MG/VIAL
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N020213
Product Number: 001
Approval Date: Sep 22, 1993
Applicant Holder Full Name: BAUSCH AND LOMB INC
Marketing Status:  Prescription
Patent and Exclusivity Information
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