anti diarrheal

Generic: loperamide hcl

Labeler: h e b
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name anti diarrheal
Generic Name loperamide hcl
Labeler h e b
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

loperamide hydrochloride 2 mg/1

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-552
Product ID 37808-552_27896be5-80e4-4821-8cbe-b1360b850e80
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA075232
Listing Expiration 2026-12-31
Marketing Start 2014-05-01

Pharmacologic Class

Classes
opioid agonist [epc] opioid agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808552
Hyphenated Format 37808-552

Supplemental Identifiers

RxCUI
978010
UNII
77TI35393C

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 anti diarrheal (source: ndc)
Generic Name loperamide hcl (source: ndc)
Application Number ANDA075232 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 12 BLISTER PACK in 1 CARTON (37808-552-53) / 1 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

loperamide hydrochloride (2 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "27896be5-80e4-4821-8cbe-b1360b850e80", "openfda": {"unii": ["77TI35393C"], "rxcui": ["978010"], "spl_set_id": ["8ecbfd81-fe45-49b4-b835-a32192de8f53"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 BLISTER PACK in 1 CARTON (37808-552-53)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "37808-552-53", "marketing_start_date": "20200220"}], "brand_name": "Anti Diarrheal", "product_id": "37808-552_27896be5-80e4-4821-8cbe-b1360b850e80", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "37808-552", "generic_name": "Loperamide HCl", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Anti Diarrheal", "active_ingredients": [{"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA075232", "marketing_category": "ANDA", "marketing_start_date": "20140501", "listing_expiration_date": "20261231"}