cycloserine

Generic: cycloserine

Labeler: dr. reddys laboratories, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cycloserine
Generic Name cycloserine
Labeler dr. reddys laboratories, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

cycloserine 250 mg/1

Manufacturer
Dr. Reddys Laboratories, Inc.

Identifiers & Regulatory

Product NDC 43598-235
Product ID 43598-235_426b2c99-759d-647a-420f-fc11b205486b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA060593
Listing Expiration 2026-12-31
Marketing Start 2023-03-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43598235
Hyphenated Format 43598-235

Supplemental Identifiers

RxCUI
197551
UNII
95IK5KI84Z

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 cycloserine (source: ndc)
Generic Name cycloserine (source: ndc)
Application Number ANDA060593 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 3 BLISTER PACK in 1 CARTON (43598-235-31) / 10 CAPSULE in 1 BLISTER PACK (43598-235-10)
source: ndc

Packages (1)

Ingredients (1)

cycloserine (250 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "426b2c99-759d-647a-420f-fc11b205486b", "openfda": {"unii": ["95IK5KI84Z"], "rxcui": ["197551"], "spl_set_id": ["8e7e2665-7a3d-3f54-9f92-5fe845f02ef9"], "manufacturer_name": ["Dr. Reddys Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (43598-235-31)  / 10 CAPSULE in 1 BLISTER PACK (43598-235-10)", "package_ndc": "43598-235-31", "marketing_start_date": "20230315"}], "brand_name": "Cycloserine", "product_id": "43598-235_426b2c99-759d-647a-420f-fc11b205486b", "dosage_form": "CAPSULE", "product_ndc": "43598-235", "generic_name": "Cycloserine", "labeler_name": "Dr. Reddys Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cycloserine", "active_ingredients": [{"name": "CYCLOSERINE", "strength": "250 mg/1"}], "application_number": "ANDA060593", "marketing_category": "ANDA", "marketing_start_date": "20230315", "listing_expiration_date": "20261231"}