prednisone delayed release

Generic: prednisone

Labeler: dr. reddys laboratories inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisone delayed release
Generic Name prednisone
Labeler dr. reddys laboratories inc.
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

prednisone 1 mg/1

Manufacturer
Dr. Reddys Laboratories Inc.

Identifiers & Regulatory

Product NDC 43598-886
Product ID 43598-886_a9e0d98c-c1bf-62b0-67b3-3b8f8313b408
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 43598886
Hyphenated Format 43598-886

Supplemental Identifiers

RxCUI
1303125 1303132
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
  • 1 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (43598-886-01) / 100 TABLET, DELAYED RELEASE in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (43598-886-30) / 30 TABLET, DELAYED RELEASE in 1 BOTTLE
source: ndc

Packages (2)

43598-886-01 1 BOTTLE in 1 CARTON (43598-886-01) / 100 TABLET, DELAYED RELEASE in 1 BOTTLE 43598-886-30 1 BOTTLE in 1 CARTON (43598-886-30) / 30 TABLET, DELAYED RELEASE in 1 BOTTLE

Ingredients (1)

prednisone (1 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": "a9e0d98c-c1bf-62b0-67b3-3b8f8313b408", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["1303125", "1303132"], "spl_set_id": ["01bdc479-1f1f-af94-837c-12e7e861321a"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Dr. Reddys Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (43598-886-01)  / 100 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "43598-886-01", "marketing_start_date": "20251215"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (43598-886-30)  / 30 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "43598-886-30", "marketing_start_date": "20251215"}], "brand_name": "Prednisone delayed release", "product_id": "43598-886_a9e0d98c-c1bf-62b0-67b3-3b8f8313b408", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "43598-886", "generic_name": "Prednisone", "labeler_name": "Dr. Reddys Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone delayed release", "active_ingredients": [{"name": "PREDNISONE", "strength": "1 mg/1"}], "application_number": "ANDA219477", "marketing_category": "ANDA", "marketing_start_date": "20251215", "listing_expiration_date": "20261231"}