Hydrochlorothiazide
- Product NDC
- 55289-136
- 11-digit product format
- 552890136
- Labeler code
- 55289
- Product ID
- 55289-136_7b1f80eb-f36b-5be4-e053-2a91aa0aac7d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA084878
- Marketing category
- ANDA
- Marketing start
- 2006-08-01
- 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
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 55289-136-01 | EA - Each | 55289-136 | f97dd172-0e5b-4038-8952-4fee35cdc92c | 1 | 2012-07-24 |
| 55289-136-06 | EA - Each | 55289-136 | 5e995471-71c2-4c99-9132-3ee92e2ef5c2 | 1 | 2012-07-24 |
| 55289-136-12 | EA - Each | 55289-136 | 076deebf-e6c6-4837-b18f-b8b2604e5a90 | 1 | 2012-07-24 |
| 55289-136-16 | EA - Each | 55289-136 | fb84836a-c2a9-4337-9866-48b43aa29780 | 1 | 2012-07-24 |
| 55289-136-20 | EA - Each | 55289-136 | 1f9fa3c8-d825-45e6-a4b8-c8cd690b9f6f | 1 | 2012-07-24 |
| 55289-136-30 | EA - Each | 55289-136 | b472960c-07f0-4d59-9f45-da09f27e8006 | 1 | 2012-07-24 |
| 55289-136-45 | EA - Each | 55289-136 | 8d6a6766-86da-401a-93cc-19efcb0893c3 | 1 | 2012-07-24 |
| 55289-136-60 | EA - Each | 55289-136 | 5230567d-427d-4a9d-bc68-ddc8b2180580 | 1 | 2012-07-24 |
| 55289-136-90 | EA - Each | 55289-136 | ad62ee85-4b5f-4328-b38e-ded61f267857 | 1 | 2012-07-24 |
| 55289-136-98 | EA - Each | 55289-136 | 0b9770fc-8020-4628-9bf4-a72ab1a87243 | 1 | 2012-07-24 |