prednisone delayed release

Generic: prednisone

Labeler: ina pharmaceutics inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisone delayed release
Generic Name prednisone
Labeler ina pharmaceutics inc
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

prednisone 2 mg/1

Manufacturer
INA Pharmaceutics Inc

Identifiers & Regulatory

Product NDC 74157-019
Product ID 74157-019_463c5b39-7eb2-d396-e063-6394a90aa451
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA219477
Listing Expiration 2026-12-31
Marketing Start 2025-12-15

Pharmacologic Class

Established (EPC)
corticosteroid [epc]
Mechanism of Action
corticosteroid hormone receptor agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 74157019
Hyphenated Format 74157-019

Supplemental Identifiers

RxCUI
1303125 1303132
UPC
0374157010305 0374157019308
UNII
VB0R961HZT
NUI
N0000175576 N0000175450

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 prednisone delayed release (source: ndc)
Generic Name prednisone (source: ndc)
Application Number ANDA219477 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (74157-019-30) / 30 TABLET, DELAYED RELEASE in 1 BOTTLE
source: ndc

Packages (1)

74157-019-30 1 BOTTLE in 1 CARTON (74157-019-30) / 30 TABLET, DELAYED RELEASE in 1 BOTTLE

Ingredients (1)

prednisone (2 mg/1)

Linked Drug Pages (1)

Prednisone delayed release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "463c5b39-7eb2-d396-e063-6394a90aa451", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0374157010305", "0374157019308"], "unii": ["VB0R961HZT"], "rxcui": ["1303125", "1303132"], "spl_set_id": ["463c7cd2-c973-5c6c-e063-6394a90a09a0"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["INA Pharmaceutics Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (74157-019-30)  / 30 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "74157-019-30", "marketing_start_date": "20251215"}], "brand_name": "Prednisone delayed release", "product_id": "74157-019_463c5b39-7eb2-d396-e063-6394a90aa451", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "74157-019", "generic_name": "Prednisone", "labeler_name": "INA Pharmaceutics Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone delayed release", "active_ingredients": [{"name": "PREDNISONE", "strength": "2 mg/1"}], "application_number": "ANDA219477", "marketing_category": "ANDA", "marketing_start_date": "20251215", "listing_expiration_date": "20261231"}