63548-1970

Generic: ibuprofen diphenhydramine citrate

Labeler: pld acquisitions llc dba avma pharma solutions
NDC Directory BULK INGREDIENT BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING Active

Drug Facts

Product Profile

Brand Name
Generic Name ibuprofen diphenhydramine citrate
Labeler pld acquisitions llc dba avma pharma solutions
Dosage Form TABLET, COATED
Active Ingredients

diphenhydramine citrate 38 mg/1, ibuprofen 200 mg/1

Identifiers & Regulatory

Product NDC 63548-1970
Product ID 63548-1970_106c6f63-1a18-4b44-a712-4f3a0115c966
Product Type BULK INGREDIENT
Marketing Category BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Listing Expiration 2027-12-31
Marketing Start 2024-11-20

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 635481970
Hyphenated Format 63548-1970

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

Generic Name ibuprofen diphenhydramine citrate (source: ndc)

Resolved Composition

Strengths
  • 38 mg/1
  • 200 mg/1
source: ndc
Packaging
  • 92463 DRUM in 1 DRUM (63548-1970-0) / 92463 TABLET, COATED in 1 DRUM
source: ndc

Packages (1)

Ingredients (2)

diphenhydramine citrate (38 mg/1) ibuprofen (200 mg/1)

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "106c6f63-1a18-4b44-a712-4f3a0115c966", "openfda": {}, "finished": false, "packaging": [{"description": "92463 DRUM in 1 DRUM (63548-1970-0)  / 92463 TABLET, COATED in 1 DRUM", "package_ndc": "63548-1970-0", "marketing_start_date": "20-NOV-24"}], "product_id": "63548-1970_106c6f63-1a18-4b44-a712-4f3a0115c966", "dosage_form": "TABLET, COATED", "product_ndc": "63548-1970", "generic_name": "Ibuprofen Diphenhydramine Citrate", "labeler_name": "PLD Acquisitions LLC DBA Avma Pharma Solutions", "product_type": "BULK INGREDIENT", "brand_name_base": null, "active_ingredients": [{"name": "DIPHENHYDRAMINE CITRATE", "strength": "38 mg/1"}, {"name": "IBUPROFEN", "strength": "200 mg/1"}], "marketing_category": "BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING", "marketing_start_date": "20241120", "listing_expiration_date": "20271231"}