miochol e

Generic: acetylcholine chloride

Labeler: bausch & lomb incorporated
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name miochol e
Generic Name acetylcholine chloride
Labeler bausch & lomb incorporated
Dosage Form KIT
Manufacturer
Bausch & Lomb Incorporated

Identifiers & Regulatory

Product NDC 24208-539
Product ID 24208-539_19c42ee4-9f98-48da-85ea-52090070c2e2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020213
Listing Expiration 2026-12-31
Marketing Start 1993-09-22

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24208539
Hyphenated Format 24208-539

Supplemental Identifiers

RxCUI
876551 876553

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name miochol e (source: ndc)
Generic Name acetylcholine chloride (source: ndc)
Application Number NDA020213 (source: ndc)

Resolved Composition

Strengths
  • 20 mg
  • 2 ml
  • 0.6 ml
source: label
Packaging
  • 1 KIT in 1 BLISTER PACK (24208-539-20) * 2 mL in 1 VIAL * 2 mL in 1 AMPULE
source: ndc

Packages (1)

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

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Miochol E ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "19c42ee4-9f98-48da-85ea-52090070c2e2", "openfda": {"rxcui": ["876551", "876553"], "spl_set_id": ["e701ef07-9499-4b56-931f-f4eb3eedbe24"], "manufacturer_name": ["Bausch & Lomb Incorporated"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 BLISTER PACK (24208-539-20)  *  2 mL in 1 VIAL *  2 mL in 1 AMPULE", "package_ndc": "24208-539-20", "marketing_start_date": "19930922"}], "brand_name": "Miochol E", "product_id": "24208-539_19c42ee4-9f98-48da-85ea-52090070c2e2", "dosage_form": "KIT", "product_ndc": "24208-539", "generic_name": "acetylcholine chloride", "labeler_name": "Bausch & Lomb Incorporated", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Miochol E", "application_number": "NDA020213", "marketing_category": "NDA", "marketing_start_date": "19930922", "listing_expiration_date": "20261231"}