Hydrochlorothiazide
- Product NDC
- 63629-7812
- 11-digit product format
- 636297812
- Labeler code
- 63629
- Product ID
- 63629-7812_e5e5d2e6-3fc7-4350-b118-a72a8c4de435
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA083177
- Marketing category
- ANDA
- Marketing start
- 1973-01-12
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63629-7812-1 | 2022-05-06 | C162847 | 48780-1 | 9d75b9d0-f9a6-f424-e053-dadaa90a57ce | dfad9b57-833f-400b-b1dd-f34a54f09a18 |
| 63629-7812-2 | 2022-05-06 | C162847 | 48780-1 | 9d75b9d0-f9a6-f424-e053-dadaa90a57ce | dfad9b57-833f-400b-b1dd-f34a54f09a18 |
| 63629-7812-3 | 2022-05-06 | C162847 | 48780-1 | 9d75b9d0-f9a6-f424-e053-dadaa90a57ce | dfad9b57-833f-400b-b1dd-f34a54f09a18 |
| 63629-7812-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-f9a6-f424-e053-dadaa90a57ce | dfad9b57-833f-400b-b1dd-f34a54f09a18 |
| 63629-7812-2 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-f9a6-f424-e053-dadaa90a57ce | dfad9b57-833f-400b-b1dd-f34a54f09a18 |
| 63629-7812-3 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-f9a6-f424-e053-dadaa90a57ce | dfad9b57-833f-400b-b1dd-f34a54f09a18 |