pilocarpine hydrochloride

Generic: pilocarpine hydrochloride

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pilocarpine hydrochloride
Generic Name pilocarpine hydrochloride
Labeler aurobindo pharma limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

pilocarpine hydrochloride 7.5 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-225
Product ID 59651-225_43f023b3-346b-4b93-95b9-ded7f37da9be
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212377
Listing Expiration 2026-12-31
Marketing Start 2019-08-13

Pharmacologic Class

Classes
cholinergic agonists [moa] cholinergic muscarinic agonists [moa] cholinergic receptor agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59651225
Hyphenated Format 59651-225

Supplemental Identifiers

RxCUI
1000913 1001004
UNII
0WW6D218XJ

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 pilocarpine hydrochloride (source: ndc)
Generic Name pilocarpine hydrochloride (source: ndc)
Application Number ANDA212377 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 7.5 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (59651-225-01)
source: ndc

Packages (1)

59651-225-01 100 TABLET, FILM COATED in 1 BOTTLE (59651-225-01)

Ingredients (1)

pilocarpine hydrochloride (7.5 mg/1)

Linked Drug Pages (1)

Pilocarpine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "43f023b3-346b-4b93-95b9-ded7f37da9be", "openfda": {"unii": ["0WW6D218XJ"], "rxcui": ["1000913", "1001004"], "spl_set_id": ["438cfaa3-b5f6-4d75-ac22-b0b4e07bb118"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59651-225-01)", "package_ndc": "59651-225-01", "marketing_start_date": "20190813"}], "brand_name": "Pilocarpine Hydrochloride", "product_id": "59651-225_43f023b3-346b-4b93-95b9-ded7f37da9be", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Agonists [MoA]", "Cholinergic Muscarinic Agonists [MoA]", "Cholinergic Receptor Agonist [EPC]"], "product_ndc": "59651-225", "generic_name": "pilocarpine hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pilocarpine Hydrochloride", "active_ingredients": [{"name": "PILOCARPINE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA212377", "marketing_category": "ANDA", "marketing_start_date": "20190813", "listing_expiration_date": "20261231"}