CHLORTHALIDONE
- Product NDC
- 50268-167
- 11-digit product format
- 502680167
- Labeler code
- 50268
- Product ID
- 50268-167_4ba86077-8f44-68da-e063-6294a90ac2ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CHLORTHALIDONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA210742
- Marketing category
- ANDA
- Marketing start
- 2019-11-12
- Substance
- CHLORTHALIDONE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide-like Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- CHLORTHALIDONE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CHLORTHALIDONE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | Q0MQD1073Q |
| Rxcui | 197499 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50268-167-11 | CHLORTHALIDONE | 1 in 1 BLISTER PACK | TABLET | 1 | | 5 |
| 50268-167-15 | CHLORTHALIDONE | 50 in 1 BOX | TABLET | 50 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50268-167 | CHLORTHALIDONE TABLET [AVPAK] | 3 | Current NDC, Legacy NDC, 2 package rows | 20220517_972b801e-c4f2-4bd6-e053-2a95a90a53bb.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50268-167-11 | 50268016711 | 1 in 1 BLISTER PACK | | | | | | Historical |
| 50268-167-15 | 50268016715 | 50 BLISTER PACK in 1 BOX (50268-167-15) / 1 TABLET in 1 BLISTER PACK (50268-167-11) | 50 blister pack | 2019-11-12 | 0000-00-00 | No | No | Current |