glycopyrrolate
Generic: glycopyrrolate
Labeler: rising pharma holdings, inc.Drug Facts
Product Profile
Brand Name
glycopyrrolate
Generic Name
glycopyrrolate
Labeler
rising pharma holdings, inc.
Dosage Form
TABLET
Routes
Active Ingredients
glycopyrrolate 2 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
16571-744
Product ID
16571-744_9f8d9c4c-f326-4784-8ea4-f791613077f7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA012827
Listing Expiration
2027-12-31
Marketing Start
2020-10-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
16571744
Hyphenated Format
16571-744
Supplemental Identifiers
RxCUI
UPC
UNII
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
glycopyrrolate (source: ndc)
Generic Name
glycopyrrolate (source: ndc)
Application Number
NDA012827 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/1
Packaging
- 30 TABLET in 1 CONTAINER (16571-744-03)
- 90 TABLET in 1 CONTAINER (16571-744-09)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9f8d9c4c-f326-4784-8ea4-f791613077f7", "openfda": {"upc": ["0316571743094"], "unii": ["V92SO9WP2I"], "rxcui": ["197738", "197739"], "spl_set_id": ["58c4cb1f-59b8-4be9-a222-2264ca077d93"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 CONTAINER (16571-744-03)", "package_ndc": "16571-744-03", "marketing_start_date": "20201006"}, {"sample": false, "description": "90 TABLET in 1 CONTAINER (16571-744-09)", "package_ndc": "16571-744-09", "marketing_start_date": "20201006"}], "brand_name": "Glycopyrrolate", "product_id": "16571-744_9f8d9c4c-f326-4784-8ea4-f791613077f7", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "16571-744", "generic_name": "Glycopyrrolate", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glycopyrrolate", "active_ingredients": [{"name": "GLYCOPYRROLATE", "strength": "2 mg/1"}], "application_number": "NDA012827", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20201006", "listing_expiration_date": "20271231"}