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Data / Drug companies / AptaPharma Inc.

AptaPharma Inc.: 30 products in the FDA NDC directory, labeler code 76281

AptaPharma Inc. (labeler code 76281) lists 30 products in the FDA National Drug Code Directory, covering 16 finished drugs by generic name. By type: 29 over the counter drugs, 1 prescription drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on May 5, 2026.

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Labeler code
76281
Products in commercial distribution
30
Packages
43
Finished drugs by generic name
16
Prescription products
1
Over the counter products
29
Flagged as original packager
29 of 29 products that carry the flag
Started marketing in the last 12 months
6
Earliest marketing start
August 21, 2013
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 drugs2686.7%
Generic drugs (ANDA)310%
New drug applications (NDA)13.3%

Products by type

TypeProductsShare
Over the counter drugs2996.7%
Prescription drugs13.3%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Liquid1860%
Suspension723.3%
Capsule, liquid filled413.3%
Solution13.3%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Prexxartan76281-155SolutionNew drug applications (NDA)May 5, 2026
Bismuth Subsalicylate Suspension Regular Strength76281-557SuspensionOver the counter monograph drugsMarch 1, 2026
DayTime High Blood Pressure Cold and Flu Relief Liquid filled Softgels76281-609Capsule, liquid filledOver the counter monograph drugsJanuary 1, 2026
Daytime Cold and Flu Relief Liquid Filled Softgels76281-604Capsule, liquid filledOver the counter monograph drugsJanuary 1, 2026
Night Time Cold and Flu relief liquid filled softgels76281-603Capsule, liquid filledOver the counter monograph drugsJanuary 1, 2026
Maximum Strength Tussin DM Liquid filled Softgels76281-601Capsule, liquid filledOver the counter monograph drugsJanuary 1, 2026
CHILDRENS COLD COUGH and SORE THROAT MIXED BERRY76281-519LiquidOver the counter monograph drugsJanuary 30, 2024
SEVERE CONGESTION and COUGH MAX76281-517LiquidOver the counter monograph drugsJanuary 30, 2024
Maximum strength Max Cold and Sinus76281-515LiquidOver the counter monograph drugsJanuary 30, 2024
Childrens mucus relief cough - cherry flavor76281-512LiquidOver the counter monograph drugsJanuary 30, 2024
Stomach Relief, Maximum Strength76281-558SuspensionOver the counter monograph drugsSeptember 30, 2020
Tussin Expectorant76281-507LiquidOver the counter monograph drugsSeptember 30, 2020
Childrens Allergy76281-505LiquidOver the counter monograph drugsSeptember 30, 2020
Tussin cf76281-504LiquidOver the counter monograph drugsSeptember 30, 2020
Tussin cough expectorant cough supressant dm76281-503LiquidOver the counter monograph drugsSeptember 30, 2020
Childrens Ibuprofen Oral Suspension Dye free76281-128SuspensionGeneric drugs (ANDA)September 30, 2020
Childrens Ibuprofen Grape76281-126SuspensionGeneric drugs (ANDA)September 30, 2020
Childrens Ibuprofen Oral Suspension76281-119SuspensionGeneric drugs (ANDA)September 30, 2020
Stomach Relief - Maximum Strength76281-538LiquidOver the counter monograph drugsOctober 1, 2018
Stomach Relief - Regular Strength76281-537LiquidOver the counter monograph drugsOctober 1, 2018
XL-3 Xtreme76281-307LiquidOver the counter monograph drugsSeptember 1, 2018
XL-3 Day Time76281-306LiquidOver the counter monograph drugsSeptember 1, 2018
Nite-Time COLD/FLU Medicine76281-501LiquidOver the counter monograph drugsMarch 9, 2018
Nighttime Sleep-Aid Non-Habit Forming76281-522LiquidOver the counter monograph drugsJanuary 1, 2018
Day-Time Cold/Flu Relief76281-506LiquidOver the counter monograph drugsJanuary 1, 2018

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