nasal decongestant maximum strength

Generic: pseudoephedrine hcl

Labeler: chain drug marketing association inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name nasal decongestant maximum strength
Generic Name pseudoephedrine hcl
Labeler chain drug marketing association inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

pseudoephedrine hydrochloride 30 mg/1

Manufacturer
CHAIN DRUG MARKETING ASSOCIATION INC

Identifiers & Regulatory

Product NDC 63868-802
Product ID 63868-802_b12d344f-09b1-4561-be1e-c3e7dc645364
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Marketing Start 1981-08-25
Marketing End 2028-02-28

Pharmacologic Class

Classes
adrenergic alpha-agonists [moa] alpha-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63868802
Hyphenated Format 63868-802

Supplemental Identifiers

RxCUI
1049160
UPC
0635515995697
UNII
6V9V2RYJ8N

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 nasal decongestant maximum strength (source: ndc)
Generic Name pseudoephedrine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (63868-802-24) / 24 TABLET, FILM COATED in 1 BLISTER PACK
  • 2 BLISTER PACK in 1 CARTON (63868-802-48) / 24 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (2)

63868-802-24 1 BLISTER PACK in 1 CARTON (63868-802-24) / 24 TABLET, FILM COATED in 1 BLISTER PACK 63868-802-48 2 BLISTER PACK in 1 CARTON (63868-802-48) / 24 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

pseudoephedrine hydrochloride (30 mg/1)

Linked Drug Pages (1)

Nasal Decongestant Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b12d344f-09b1-4561-be1e-c3e7dc645364", "openfda": {"upc": ["0635515995697"], "unii": ["6V9V2RYJ8N"], "rxcui": ["1049160"], "spl_set_id": ["db81e32b-0cad-400b-8479-a3b51de92b12"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (63868-802-24)  / 24 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "63868-802-24", "marketing_end_date": "20280228", "marketing_start_date": "19810825"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (63868-802-48)  / 24 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "63868-802-48", "marketing_end_date": "20280228", "marketing_start_date": "19810825"}], "brand_name": "Nasal Decongestant Maximum Strength", "product_id": "63868-802_b12d344f-09b1-4561-be1e-c3e7dc645364", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "63868-802", "generic_name": "Pseudoephedrine HCl", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Nasal Decongestant", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20280228", "marketing_start_date": "19810825"}