Prescription drug · ANDA
Hydrochlorothiazide NDC 63629-8992
Hydrochlorothiazide 50 mg/1 · Tablet · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 63629-8992-1 | 63629899201 | 30 TABLET in 1 BOTTLE, PLASTIC (63629-8992-1)Marketed from Dec 7, 2021 | |
| 63629-8992-2 | 63629899202 | 60 TABLET in 1 BOTTLE, PLASTIC (63629-8992-2)Marketed from Dec 7, 2021 | |
| 63629-8992-3 | 63629899203 | 90 TABLET in 1 BOTTLE, PLASTIC (63629-8992-3)Marketed from Dec 7, 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 — 50 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Bryant Ranch Prepack
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 040412
- Marketing start
- Listing expires
- Other FDA classes
- Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
- Identifiers
- Product ID 63629-8992_61f76c85-a81f-44a7-bbd5-96b8a952f356SPL ID 61f76c85-a81f-44a7-bbd5-96b8a952f356SPL set ID 4c3403a6-da6a-4f37-bc7e-9fe0aa284305RxCUI 197770UNII 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
N463629899201followed by a unit qualifier and the quantityPackage 63629-8992-01. 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
Label details couldn’t be retrieved right now. Open the label on DailyMed.
Other NDCs under ANDA 040412
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 50 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-1451 |
| Hydrochlorothiazide | Hydrochlorothiazide 50 mg/1 | TabletOral | Bryant Ranch Prepack | 72162-1357 |
| Hydrochlorothiazide | Hydrochlorothiazide 25 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-1481 |
| Hydrochlorothiazide | Hydrochlorothiazide 25 mg/1 | TabletOral | American Health Packaging | 60687-593 |
| Hydrochlorothiazide | Hydrochlorothiazide 50 mg/1 | TabletOral | Bryant Ranch Prepack | 63629-1220 |
| Hydrochlorothiazide | Hydrochlorothiazide 25 mg/1 | TabletOral | Bryant Ranch Prepack | 63629-1218 |
| Hydrochlorothiazide | Hydrochlorothiazide 25 mg/1 | TabletOral | Solco Healthcare U.S., LLC | 43547-397 |
| Hydrochlorothiazide | Hydrochlorothiazide 50 mg/1 | TabletOral | Solco Healthcare U.S., LLC | 43547-398 |