sulfamethoxazole and trimethoprim
Generic: sulfamethoxazole and trimethoprim
Labeler: sportpharm llcDrug Facts
Product Profile
Brand Name
sulfamethoxazole and trimethoprim
Generic Name
sulfamethoxazole and trimethoprim
Labeler
sportpharm llc
Dosage Form
TABLET
Routes
Active Ingredients
sulfamethoxazole 800 mg/1, trimethoprim 160 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
85766-015
Product ID
85766-015_49ef26b9-b7b9-bfa8-e063-6394a90a0c50
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090624
Listing Expiration
2027-12-31
Marketing Start
2010-02-16
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
85766015
Hyphenated Format
85766-015
Supplemental Identifiers
RxCUI
UNII
NUI
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
sulfamethoxazole and trimethoprim (source: ndc)
Generic Name
sulfamethoxazole and trimethoprim (source: ndc)
Application Number
ANDA090624 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 800 mg/1
- 160 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (85766-015-01)
- 500 TABLET in 1 BOTTLE (85766-015-05)
- 6 TABLET in 1 BOTTLE (85766-015-06)
- 10 TABLET in 1 BOTTLE (85766-015-10)
- 14 TABLET in 1 BOTTLE (85766-015-14)
- 20 TABLET in 1 BOTTLE (85766-015-20)
- 28 TABLET in 1 BOTTLE (85766-015-28)
- 30 TABLET in 1 BOTTLE (85766-015-30)
Packages (8)
85766-015-01
100 TABLET in 1 BOTTLE (85766-015-01)
85766-015-05
500 TABLET in 1 BOTTLE (85766-015-05)
85766-015-06
6 TABLET in 1 BOTTLE (85766-015-06)
85766-015-10
10 TABLET in 1 BOTTLE (85766-015-10)
85766-015-14
14 TABLET in 1 BOTTLE (85766-015-14)
85766-015-20
20 TABLET in 1 BOTTLE (85766-015-20)
85766-015-28
28 TABLET in 1 BOTTLE (85766-015-28)
85766-015-30
30 TABLET in 1 BOTTLE (85766-015-30)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
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