Prescription drug · ANDA
Hydrochlorothiazide NDC 71335-1713
Hydrochlorothiazide 12.5 mg/1 · Capsule · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71335-1713-1 | 7133517130171335171301 | 30 CAPSULE in 1 BOTTLE (71335-1713-1)Marketed from Jan 15, 2021 | |
| 71335-1713-2 | 7133517130271335171302 | 10 CAPSULE in 1 BOTTLE (71335-1713-2)Marketed from Apr 12, 2021 | |
| 71335-1713-3 | 7133517130371335171303 | 90 CAPSULE in 1 BOTTLE (71335-1713-3)Marketed from Oct 2, 2020 | |
| 71335-1713-4 | 7133517130471335171304 | 100 CAPSULE in 1 BOTTLE (71335-1713-4)Marketed from Feb 12, 2021 | |
| 71335-1713-5 | 7133517130571335171305 | 60 CAPSULE in 1 BOTTLE (71335-1713-5)Marketed from Dec 10, 2024 | |
| 71335-1713-6 | 7133517130671335171306 | 120 CAPSULE in 1 BOTTLE (71335-1713-6)Marketed from Aug 12, 2021 | |
| 71335-1713-7 | 7133517130771335171307 | 7 CAPSULE in 1 BOTTLE (71335-1713-7)Marketed from Jul 2, 2021 | |
| 71335-1713-8 | 7133517130871335171308 | 15 CAPSULE in 1 BOTTLE (71335-1713-8)Marketed from Dec 10, 2024 | |
| 71335-1713-9 | 7133517130971335171309 | 14 CAPSULE in 1 BOTTLE (71335-1713-9)Marketed from Jul 2, 2021 |
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
- Bryant Ranch PrepackNDC labeler code 71335
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 203561
- Marketing start
- Listing expires
- Other FDA classes
- Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
- Identifiers
- Product ID 71335-1713_c545f051-9fce-4a1f-b98b-6ef78b63a7edSPL ID c545f051-9fce-4a1f-b98b-6ef78b63a7edSPL set ID 2b21f3fc-4164-401a-803e-b982dea97e19RxCUI 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
N471335171301followed by a unit qualifier and the quantityPackage 71335-1713-01. 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 Hydrochlorothiazide capsules, USP are indicated in the management of hypertension either as the sole therapeutic agent, or in combination with other antihypertensives. Unlike potassium sparing combination diuretic products, hydrochlorothiazide capsules, USP may be used in those patients in whom the development of hyperkalemia cannot be risked, including patients taking ACE inhibitors. Usage in Pregnancy: The routine use of diuretics in an otherwise healthy woman is inappropriate and exposes mother and fetus to unnecessary hazard. Diuretics do not prevent development of toxemia of pregnancy, and there is no satisfactory evidence that they are useful in the treatment of d…
Excerpt only. Read the full label for complete information.
About NDC 71335-1713
- What is NDC 71335-1713?
- 71335-1713 is the product NDC for Hydrochlorothiazide, Hydrochlorothiazide 12.5 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 9 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?
- Bryant Ranch Prepack, NDC labeler code 71335. 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 203561
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 | NCS HealthCare of KY, LLC dba Vangard Labs | 0615-8344 |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | CapsuleOral | A-S Medication Solutions | 50090-6987 |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | CapsuleOral | A-S Medication Solutions | 50090-6988 |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | CapsuleOral | ScieGen Pharmaceuticals Inc | 50228-146 |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | CapsuleOral | AvPAK | 50268-404 |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | CapsuleOral | Northwind Health Company, LLC | 51655-616 |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | CapsuleOral | Bryant Ranch Prepack | 63629-8498 |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | CapsuleOral | Preferred Pharmaceuticals, Inc. | 68788-7683 |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | CapsuleOral | Westminster Pharmaceuticals, LLC | 69367-219 |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | CapsuleOral | REMEDYREPACK INC. | 70518-2550 |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | CapsuleOral | Proficient Rx LP | 71205-589 |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | CapsuleOral | Proficient Rx LP | 71205-980 |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | CapsuleOral | Aphena Pharma Solutions - Tennessee, LLC | 71610-500 |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | CapsuleOral | Aphena Pharma Solutions - Tennessee, LLC | 71610-697 |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | CapsuleOral | Bryant Ranch Prepack | 72162-1528 |
| Hydrochlorothiazide | Hydrochlorothiazide 12.5 mg/1 | CapsuleOral | PD-Rx Pharmaceuticals, Inc. | 72789-176 |