buspirone hydrochloride

Generic: buspirone hydrochloride

Labeler: strides pharma inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buspirone hydrochloride
Generic Name buspirone hydrochloride
Labeler strides pharma inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

buspirone hydrochloride 10 mg/1

Manufacturer
Strides Pharma Inc.

Identifiers & Regulatory

Product NDC 42543-742
Product ID 42543-742_2357cfc5-edfb-40d5-8b55-2c7f11704091
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202330
Listing Expiration 2027-12-31
Marketing Start 2021-04-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42543742
Hyphenated Format 42543-742

Supplemental Identifiers

RxCUI
866018 866083 866090 866094 866111
UPC
0342543744035 0342543787063 0342543742079 0342543741072 0342543743182
UNII
207LT9J9OC

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 buspirone hydrochloride (source: ndc)
Generic Name buspirone hydrochloride (source: ndc)
Application Number ANDA202330 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (42543-742-06)
  • 500 TABLET in 1 BOTTLE (42543-742-07)
  • 1000 TABLET in 1 BOTTLE (42543-742-08)
source: ndc

Packages (3)

42543-742-06 100 TABLET in 1 BOTTLE (42543-742-06) 42543-742-07 500 TABLET in 1 BOTTLE (42543-742-07) 42543-742-08 1000 TABLET in 1 BOTTLE (42543-742-08)

Ingredients (1)

buspirone hydrochloride (10 mg/1)

Linked Drug Pages (1)

Buspirone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2357cfc5-edfb-40d5-8b55-2c7f11704091", "openfda": {"upc": ["0342543744035", "0342543787063", "0342543742079", "0342543741072", "0342543743182"], "unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094", "866111"], "spl_set_id": ["cb0091ad-97f6-431b-b2b9-e03171eed274"], "manufacturer_name": ["Strides Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42543-742-06)", "package_ndc": "42543-742-06", "marketing_start_date": "20210401"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (42543-742-07)", "package_ndc": "42543-742-07", "marketing_start_date": "20210401"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (42543-742-08)", "package_ndc": "42543-742-08", "marketing_start_date": "20210401"}], "brand_name": "Buspirone Hydrochloride", "product_id": "42543-742_2357cfc5-edfb-40d5-8b55-2c7f11704091", "dosage_form": "TABLET", "product_ndc": "42543-742", "generic_name": "Buspirone Hydrochloride", "labeler_name": "Strides Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA202330", "marketing_category": "ANDA", "marketing_start_date": "20210401", "listing_expiration_date": "20271231"}