Data / Drug companies / Creekwood Pharmaceuticals LLC
Creekwood Pharmaceuticals LLC: 38 products in the FDA NDC directory, labeler code 82619
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Creekwood Pharmaceuticals LLC (labeler code 82619) lists 38 products in the FDA National Drug Code Directory, covering 10 finished drugs by generic name. By type: 38 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on August 29, 2026.
The request: Watch Creekwood Pharmaceuticals LLC (FDA labeler code 82619): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 82619
- Products in commercial distribution
- 38
- Packages
- 83
- Finished drugs by generic name
- 10
- Prescription products
- 38
- Over the counter products
- 0
- Controlled substance products
- Schedule V 8
- Flagged as original packager
- 38 of 38 products that carry the flag
- Started marketing in the last 12 months
- 18
- Earliest marketing start
- December 31, 2012
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 38 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 38 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Pregabalin | 8 | 54 |
| Atomoxetine | 7 | 19 |
| Haloperidol | 6 | 32 |
| Gabapentin | 5 | 91 |
| Propranolol hydrochloride | 4 | 51 |
| Fenofibrate | 2 | 56 |
| Rizatriptan benzoate | 2 | 25 |
| Silodosin | 2 | 15 |
| Nitrofurantoin (monohydrate/macrocrystals) | 1 | 25 |
| Hydroxychloroquine sulfate | 1 | 33 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Capsule | 21 | 55.3% |
| Tablet | 13 | 34.2% |
| Capsule, extended release | 4 | 10.5% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Propranolol Hydrochloride | 82619-135 | Capsule, extended release | Generic drugs (ANDA) | August 29, 2026 |
| Propranolol Hydrochloride | 82619-134 | Capsule, extended release | Generic drugs (ANDA) | August 29, 2026 |
| Propranolol Hydrochloride | 82619-133 | Capsule, extended release | Generic drugs (ANDA) | August 29, 2026 |
| Propranolol Hydrochloride | 82619-132 | Capsule, extended release | Generic drugs (ANDA) | August 29, 2026 |
| Atomoxetine | 82619-121 | Capsule | Generic drugs (ANDA) | July 6, 2026 |
| Atomoxetine | 82619-120 | Capsule | Generic drugs (ANDA) | July 6, 2026 |
| Atomoxetine | 82619-119 | Capsule | Generic drugs (ANDA) | July 6, 2026 |
| Atomoxetine | 82619-118 | Capsule | Generic drugs (ANDA) | July 6, 2026 |
| Atomoxetine | 82619-117 | Capsule | Generic drugs (ANDA) | July 6, 2026 |
| Atomoxetine | 82619-116 | Capsule | Generic drugs (ANDA) | July 6, 2026 |
| Atomoxetine | 82619-115 | Capsule | Generic drugs (ANDA) | July 6, 2026 |
| Nitrofurantoin (monohydrate/macrocrystals) | 82619-147 | Capsule | Generic drugs (ANDA) | April 20, 2026 |
| Haloperidol | 82619-110 | Tablet | Generic drugs (ANDA) | January 5, 2026 |
| Haloperidol | 82619-109 | Tablet | Generic drugs (ANDA) | January 5, 2026 |
| Haloperidol | 82619-108 | Tablet | Generic drugs (ANDA) | January 5, 2026 |
| Haloperidol | 82619-107 | Tablet | Generic drugs (ANDA) | January 5, 2026 |
| Haloperidol | 82619-106 | Tablet | Generic drugs (ANDA) | January 5, 2026 |
| Haloperidol | 82619-105 | Tablet | Generic drugs (ANDA) | January 5, 2026 |
| Hydroxychloroquine sulfate | 82619-131 | Tablet | Generic drugs (ANDA) | May 8, 2025 |
| Silodosin | 82619-114 | Capsule | Generic drugs (ANDA) | November 14, 2024 |
| Silodosin | 82619-113 | Capsule | Generic drugs (ANDA) | November 14, 2024 |
| Pregabalin | 82619-129 | Capsule | Generic drugs (ANDA) | September 20, 2024 |
| Pregabalin | 82619-128 | Capsule | Generic drugs (ANDA) | September 20, 2024 |
| Pregabalin | 82619-127 | Capsule | Generic drugs (ANDA) | September 20, 2024 |
| Pregabalin | 82619-126 | Capsule | Generic drugs (ANDA) | September 20, 2024 |
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.