Data / Drug companies / Aci Healthcare USA, Inc.
Aci Healthcare USA, Inc.: 10 products in the FDA NDC directory, labeler code 71093
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Aci Healthcare USA, Inc. (labeler code 71093) lists 10 products in the FDA National Drug Code Directory, covering 3 finished drugs by generic name. By type: 10 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on September 24, 2020.
The request: Watch Aci Healthcare USA, Inc. (FDA labeler code 71093): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 71093
- Products in commercial distribution
- 10
- Packages
- 16
- Finished drugs by generic name
- 3
- Prescription products
- 10
- Over the counter products
- 0
- Controlled substance products
- Schedule IV 2
- Flagged as original packager
- 10 of 10 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- November 29, 2017
- 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) | 10 | 100% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 10 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Quetiapine | 5 | 30 |
| Metformin hydrochloride | 3 | 79 |
| Zolpidem tartrate | 2 | 38 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated, extended release | 5 | 50% |
| Tablet | 5 | 50% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Zolpidem | 71093-156 | Tablet | Generic drugs (ANDA) | September 24, 2020 |
| Zolpidem | 71093-155 | Tablet | Generic drugs (ANDA) | September 24, 2020 |
| Metformin hydrochloride | 71093-134 | Tablet | Generic drugs (ANDA) | January 15, 2018 |
| Metformin hydrochloride | 71093-133 | Tablet | Generic drugs (ANDA) | January 15, 2018 |
| Metformin hydrochloride | 71093-132 | Tablet | Generic drugs (ANDA) | January 15, 2018 |
| Quetiapine Extended Release | 71093-139 | Tablet, film coated, extended release | Generic drugs (ANDA) | November 29, 2017 |
| Quetiapine Extended Release | 71093-138 | Tablet, film coated, extended release | Generic drugs (ANDA) | November 29, 2017 |
| Quetiapine Extended Release | 71093-137 | Tablet, film coated, extended release | Generic drugs (ANDA) | November 29, 2017 |
| Quetiapine Extended Release | 71093-136 | Tablet, film coated, extended release | Generic drugs (ANDA) | November 29, 2017 |
| Quetiapine Extended Release | 71093-135 | Tablet, film coated, extended release | Generic drugs (ANDA) | November 29, 2017 |
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.