Data / Drug companies / Velocity Pharma LLC
Velocity Pharma LLC: 7 products in the FDA NDC directory, labeler code 76168
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Velocity Pharma LLC (labeler code 76168) lists 7 products in the FDA National Drug Code Directory, covering 6 finished drugs by generic name. By type: 7 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on July 2, 2019.
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- Labeler code
- 76168
- Products in commercial distribution
- 7
- Packages
- 12
- Finished drugs by generic name
- 6
- Prescription products
- 0
- Over the counter products
- 7
- Flagged as original packager
- 7 of 7 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- December 5, 2012
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Over the counter monograph drugs | 6 | 85.7% |
| Generic drugs (ANDA) | 1 | 14.3% |
Products by type
| Type | Products | Share |
|---|---|---|
| Over the counter drugs | 7 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Diphenhydramine hydrochloride | 2 | 127 |
| Acetaminophen,dextromethorphan,doxylamine | 1 | 1 |
| Acetaminophen pm | 1 | 2 |
| Diphenhydramine | 1 | 2 |
| Acetaminophen | 1 | 214 |
| Levocetirizine dihydrochloride | 1 | 52 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet | 4 | 57.1% |
| Capsule, liquid filled | 2 | 28.6% |
| Tablet, film coated | 1 | 14.3% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Histamine-1 Receptor Antagonist | 5 |
| Antihistamine | 1 |
| Sigma-1 Agonist | 1 |
| Uncompetitive N-methyl-D-aspartate Receptor Antagonist | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Allergy Relief 24HR | 76168-501 | Tablet | Generic drugs (ANDA) | July 2, 2019 |
| Allergy | 76168-121 | Tablet | Over the counter monograph drugs | May 14, 2018 |
| Acetaminophen | 76168-120 | Tablet | Over the counter monograph drugs | May 14, 2018 |
| Sleep Aid | 76168-015 | Tablet, film coated | Over the counter monograph drugs | May 14, 2018 |
| NightTime Cold and Flu | 76168-056 | Capsule, liquid filled | Over the counter monograph drugs | May 1, 2014 |
| Nightime Sleep Aid | 76168-065 | Capsule, liquid filled | Over the counter monograph drugs | March 31, 2014 |
| Pain Relief PM | 76168-119 | Tablet | Over the counter monograph drugs | December 5, 2012 |
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.