CHLORTHALIDONE
- Product NDC
- 69776-218
- 11-digit product format
- 697760218
- Labeler code
- 69776
- Product ID
- 69776-218_ebc34409-3e03-deff-e053-2995a90af98d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CHLORTHALIDONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sunny Pharmtech Inc.
- Application
- ANDA209068
- Marketing category
- ANDA
- Marketing start
- 2022-10-03
- Marketing end
- 2022-10-31
- Substance
- CHLORTHALIDONE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide-like Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record