bacitracin
Generic: bacitracin
Labeler: dynarex corporationDrug Facts
Product Profile
Brand Name
bacitracin
Generic Name
bacitracin
Labeler
dynarex corporation
Dosage Form
OINTMENT
Routes
Active Ingredients
bacitracin 500 [USP'U]/1000mg
Manufacturer
Identifiers & Regulatory
Product NDC
67777-116
Product ID
67777-116_275e9fdf-28d0-498a-e063-6294a90a7eea
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M004
Listing Expiration
2026-12-31
Marketing Start
2016-09-12
Pharmacologic Class
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
67777116
Hyphenated Format
67777-116
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
bacitracin (source: ndc)
Generic Name
bacitracin (source: ndc)
Application Number
M004 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 [USP'U]/1000mg
Packaging
- 1728 BOX in 1 CASE (67777-116-10) / 144 PACKET in 1 BOX (67777-116-11) / 900 mg in 1 PACKET
- 72 TUBE in 1 CASE (67777-116-20) / 14000 mg in 1 TUBE (67777-116-21)
- 72 BOX in 1 CASE (67777-116-30) / 1 TUBE in 1 BOX (67777-116-31) / 28400 mg in 1 TUBE
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "275e9fdf-28d0-498a-e063-6294a90a7eea", "openfda": {"nui": ["N0000008479"], "upc": ["0616784116228", "0616784116310", "0616784116129"], "unii": ["58H6RWO52I"], "rxcui": ["1648110"], "spl_set_id": ["7f8752c7-6839-261d-e053-2991aa0a0c30"], "pharm_class_pe": ["Decreased Cell Wall Synthesis & Repair [PE]"], "manufacturer_name": ["Dynarex Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1728 BOX in 1 CASE (67777-116-10) / 144 PACKET in 1 BOX (67777-116-11) / 900 mg in 1 PACKET", "package_ndc": "67777-116-10", "marketing_start_date": "20160912"}, {"sample": false, "description": "72 TUBE in 1 CASE (67777-116-20) / 14000 mg in 1 TUBE (67777-116-21)", "package_ndc": "67777-116-20", "marketing_start_date": "20160912"}, {"sample": false, "description": "72 BOX in 1 CASE (67777-116-30) / 1 TUBE in 1 BOX (67777-116-31) / 28400 mg in 1 TUBE", "package_ndc": "67777-116-30", "marketing_start_date": "20160912"}], "brand_name": "Bacitracin", "product_id": "67777-116_275e9fdf-28d0-498a-e063-6294a90a7eea", "dosage_form": "OINTMENT", "pharm_class": ["Decreased Cell Wall Synthesis & Repair [PE]"], "product_ndc": "67777-116", "generic_name": "Bacitracin", "labeler_name": "Dynarex Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bacitracin", "active_ingredients": [{"name": "BACITRACIN", "strength": "500 [USP'U]/1000mg"}], "application_number": "M004", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160912", "listing_expiration_date": "20261231"}