Package 71930-037-52

Brand: Labetalol Hydrochloride

Generic: Labetalol Hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71930-037-52
Digits Only 7193003752
Product NDC 71930-037
Product ID 71930-037_d923d8d6-a2c9-4afa-a1c2-67afddd5af1a
Description

500 TABLET, FILM COATED in 1 BOTTLE (71930-037-52)

Marketing

Marketing Status
Marketed Since 2019-05-24
Brand Labetalol Hydrochloride
Generic Labetalol Hydrochloride
Sample Package No

Linked Drug Pages (1)

Labetalol Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d923d8d6-a2c9-4afa-a1c2-67afddd5af1a", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896758", "896762", "896766"], "spl_set_id": ["891c42c0-6071-5d85-e053-2995a90a4294"], "manufacturer_name": ["Eywa Pharma Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71930-037-12)", "package_ndc": "71930-037-12", "marketing_start_date": "20190524"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (71930-037-52)", "package_ndc": "71930-037-52", "marketing_start_date": "20190524"}], "brand_name": "Labetalol Hydrochloride", "product_id": "71930-037_d923d8d6-a2c9-4afa-a1c2-67afddd5af1a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71930-037", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Eywa Pharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA207863", "marketing_category": "ANDA", "marketing_start_date": "20190524", "listing_expiration_date": "20261231"}