Prescription drug · ANDA
Hydrochlorothiazide NDC 68788-8862
Hydrochlorothiazide 12.5 mg/1 · Capsule · Oral · Preferred Pharmaceuticals Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 68788-8862-1 | 6878888620168788886201 | 100 CAPSULE in 1 BOTTLE (68788-8862-1)Marketed from Apr 29, 2025 | |
| 68788-8862-3 | 6878888620368788886203 | 30 CAPSULE in 1 BOTTLE (68788-8862-3)Marketed from Apr 29, 2025 | |
| 68788-8862-6 | 6878888620668788886206 | 60 CAPSULE in 1 BOTTLE (68788-8862-6)Marketed from Apr 29, 2025 | |
| 68788-8862-7 | 6878888620768788886207 | 7 CAPSULE in 1 BOTTLE (68788-8862-7)Marketed from Apr 29, 2025 | |
| 68788-8862-9 | 6878888620968788886209 | 90 CAPSULE in 1 BOTTLE (68788-8862-9)Marketed from Apr 29, 2025 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Hydrochlorothiazide
- Generic name (nonproprietary)
- hydrochlorothiazide
- Active ingredients
- Hydrochlorothiazide — 12.5 mg/1
- Dosage form
- Capsule
- Route
- Oral
- Labeler
- Preferred Pharmaceuticals Inc.NDC labeler code 68788
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 078164
- Marketing start
- Listing expires
- Other FDA classes
- Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
- Identifiers
- Product ID 68788-8862_82ad0fdf-5d47-4c2d-883b-f28b2d3fb6b0SPL ID 82ad0fdf-5d47-4c2d-883b-f28b2d3fb6b0SPL set ID 82ad0fdf-5d47-4c2d-883b-f28b2d3fb6b0RxCUI 199903UNII 0J48LPH2TH
- Pharmacologic class
- Thiazide Diuretic
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N468788886201followed by a unit qualifier and the quantityPackage 68788-8862-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATIONS AND USAGE Hydrochloro‑thiazide capsules are indicated in the management of hypertension either as the sole therapeutic agent, or in combination with other antihypertensives. Unlike potassium sparing combina‑tion diuretic products, hydrochloro‑thiazide capsules may be used in those patients in whom the development of hyperkalemia cannot be risked, including patients taking ACE inhibitors. Usage in Pregnancy: The rou‑tine use of diuretics in an otherwise healthy woman is inappropriate and exposes mother and fetus to unneces‑sary hazard. Diuretics do not prevent development of tox‑emia of pregnancy, and there is no satisfactory evidence that they are useful in the treatment of devel…
Excerpt only. Read the full label for complete information.
About NDC 68788-8862
- What is NDC 68788-8862?
- 68788-8862 is the product NDC for Hydrochlorothiazide, Hydrochlorothiazide 12.5 mg/1 capsule, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 5 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Hydrochlorothiazide.
- What is the active ingredient?
- Hydrochlorothiazide.
- Who is the labeler?
- Preferred Pharmaceuticals Inc., NDC labeler code 68788. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Hydrochlorothiazide?
- 166 other product NDCs are listed under this name. See all Hydrochlorothiazide NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Hydrochlorothiazide products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Hydrochlorothiazide | Hydrochlorothiazide 50 mg/5mL | SolutionOral | Advagen Pharma Ltd | 72888-491 | 72888-0491-01 |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | TabletOral | Teva Pharmaceuticals, Inc. | 0480-3444 | 00480-3444-10 |
| hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | CapsuleOral | Preferred Pharmaceuticals Inc. | 68788-4192 | 68788-4192-0168788-4192-0368788-4192-06+2 more |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4736 | 70518-4736-00 |
| Hydrochlorothiazide | Hydrochlorothiazide 25 mg/1 | TabletOral | Unit Dose Solutions, Inc. | 87441-038 | 87441-0038-01 |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | TabletOral | Coupler LLC | 67046-1664 | 67046-1664-03 |
| Hydrochlorothiazide | Hydrochlorothiazide 25 mg/1 | TabletOral | American Health Packaging | 60687-894 | 60687-0894-01 |
| Hydrochlorothiazide | Hydrochlorothiazide 50 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4525 | 70518-4525-00 |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4466 | 70518-4466-0070518-4466-01 |
| Hydrochlorothiazide | Hydrochlorothiazide 25 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4359 | 70518-4359-0070518-4359-0170518-4359-02+2 more |
Other NDCs under ANDA 078164
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | CapsuleOral | Rising Pharma Holdings, Inc. | 57237-002 |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | CapsuleOral | Bryant Ranch Prepack | 71335-0770 |