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Data / Drug companies / Advance Pharmaceutical Inc.

Advance Pharmaceutical Inc.: 24 products in the FDA NDC directory, labeler code 17714

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Advance Pharmaceutical Inc. (labeler code 17714) lists 24 products in the FDA National Drug Code Directory, covering 12 finished drugs by generic name. By type: 24 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on November 11, 2021.

The request: Watch Advance Pharmaceutical Inc. (FDA labeler code 17714): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
17714
Products in commercial distribution
24
Packages
38
Finished drugs by generic name
12
Prescription products
0
Over the counter products
24
Flagged as original packager
24 of 24 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
April 15, 1988
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Over the counter monograph drugs24100%

Products by type

TypeProductsShare
Over the counter drugs24100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

Dosage forms

Dosage formProductsShare
Tablet1458.3%
Tablet, chewable729.2%
Capsule28.3%
Gel14.2%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Simethicone Certified Plus17714-076GelOver the counter monograph drugsNovember 11, 2021
Mucus Relief Cough and Congestion DM17714-150TabletOver the counter monograph drugsAugust 1, 2017
Mucus Relief17714-152TabletOver the counter monograph drugsNovember 1, 2016
Meclizine HCL 12.5 mg17714-117TabletOver the counter monograph drugsJuly 1, 2013
Meclizine HCL17714-115Tablet, chewableOver the counter monograph drugsJuly 1, 2013
Simethicone17714-040Tablet, chewableOver the counter monograph drugsNovember 1, 2012
Diphenhydramine Hydrochloride17714-023TabletOver the counter monograph drugsSeptember 1, 2012
Antacid17714-041Tablet, chewableOver the counter monograph drugsNovember 30, 2007
Diphenhydramine Hydrochloride17714-135TabletOver the counter monograph drugsSeptember 26, 2006
Acetaminophen pm17714-133TabletOver the counter monograph drugsJanuary 9, 2002
Pepto Relief17714-045Tablet, chewableOver the counter monograph drugsJanuary 9, 2002
Anti Allergy17714-016TabletOver the counter monograph drugsJanuary 9, 2002
Aspirin17714-010TabletOver the counter monograph drugsJanuary 9, 2002
Gas Relief17714-019Tablet, chewableOver the counter monograph drugsNovember 4, 1999
Aspirin17714-121TabletOver the counter monograph drugsJune 12, 1999
Antacid17714-043Tablet, chewableOver the counter monograph drugsJanuary 26, 1996
Aspirin17714-011TabletOver the counter monograph drugsMay 8, 1990
Antacid17714-025TabletOver the counter monograph drugsApril 6, 1990
Apap17714-014TabletOver the counter monograph drugsJanuary 14, 1990
Diphenhydramine Hydrochloride17714-021CapsuleOver the counter monograph drugsOctober 5, 1989
Diphenhydramine Hydrochloride17714-020CapsuleOver the counter monograph drugsSeptember 12, 1989
Apap17714-013TabletOver the counter monograph drugsFebruary 5, 1989
Acetaminophen17714-012TabletOver the counter monograph drugsFebruary 5, 1989
Aspirin17714-009Tablet, chewableOver the counter monograph drugsApril 15, 1988

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.