Data / Drug companies / Centaur Pharmaceuticals Private Limited
Centaur Pharmaceuticals Private Limited: 19 products in the FDA NDC directory, labeler code 64330
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Centaur Pharmaceuticals Private Limited (labeler code 64330) lists 19 products in the FDA National Drug Code Directory, covering 1 finished drug by generic name. By type: 12 bulk ingredients, 6 prescription drugs. Its main marketing category is bulk ingredients. The newest product started marketing on June 6, 2022.
The request: Watch Centaur Pharmaceuticals Private Limited (FDA labeler code 64330): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 64330
- Products in commercial distribution
- 19
- Packages
- 168
- Finished drugs by generic name
- 1
- Prescription products
- 6
- Over the counter products
- 0
- Controlled substance products
- Schedule IV 8
- Flagged as original packager
- 6 of 6 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- January 23, 2003
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Bulk ingredients | 12 | 63.2% |
| Generic drugs (ANDA) | 6 | 31.6% |
| Drugs for further processing | 1 | 5.3% |
Products by type
| Type | Products | Share |
|---|---|---|
| Bulk ingredients | 12 | 63.2% |
| Prescription drugs | 6 | 31.6% |
| Drugs for further processing | 1 | 5.3% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Amitriptyline hydrochloride | 6 | 35 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Powder | 12 | 63.2% |
| Tablet | 6 | 31.6% |
| Granule | 1 | 5.3% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Tricyclic Antidepressant | 6 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Amitriptyline Hydrochloride | 64330-635 | Tablet | Generic drugs (ANDA) | June 6, 2022 |
| Amitriptyline Hydrochloride | 64330-634 | Tablet | Generic drugs (ANDA) | June 6, 2022 |
| Amitriptyline Hydrochloride | 64330-633 | Tablet | Generic drugs (ANDA) | June 6, 2022 |
| Amitriptyline Hydrochloride | 64330-632 | Tablet | Generic drugs (ANDA) | June 6, 2022 |
| Amitriptyline Hydrochloride | 64330-631 | Tablet | Generic drugs (ANDA) | June 6, 2022 |
| Amitriptyline Hydrochloride | 64330-630 | Tablet | Generic drugs (ANDA) | June 6, 2022 |
| Pyridostigmine bromide | 64330-670 | Granule | Drugs for further processing | January 28, 2019 |
| Pindolol | 64330-109 | Powder | Bulk ingredients | January 5, 2018 |
| Zaleplon | 64330-054 | Powder | Bulk ingredients | January 5, 2018 |
| Chlordiazepoxide | 64330-082 | Powder | Bulk ingredients | October 1, 2015 |
| Metolazone | 64330-115 | Powder | Bulk ingredients | July 29, 2015 |
| Clobazam | 64330-110 | Powder | Bulk ingredients | February 23, 2015 |
| Loxapine succinate | 64330-112 | Powder | Bulk ingredients | February 18, 2015 |
| Timolol maleate | 64330-014 | Powder | Bulk ingredients | March 11, 2010 |
| Clonazepam | 64330-019 | Powder | Bulk ingredients | February 17, 2009 |
| Oxazepam | 64330-015 | Powder | Bulk ingredients | September 30, 2008 |
| Diazepam | 64330-010 | Powder | Bulk ingredients | July 24, 2008 |
| Alprazolam | 64330-013 | Powder | Bulk ingredients | August 30, 2007 |
| Lorazepam | 64330-020 | Powder | Bulk ingredients | January 23, 2003 |
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.