CHLORTHALIDONE 50MG
- Product NDC
- 73141-875
- 11-digit product format
- 731410875
- Labeler code
- 73141
- Product ID
- 73141-875_e35436a4-beb4-4dc8-e053-2995a90aa8fc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CHLORTHALIDONE 50MG
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A2A Integrated Pharmaceuticals, LLC
- Application
- ANDA212875
- Marketing category
- ANDA
- Marketing start
- 2022-09-20
- Marketing end
- 0000-00-00
- Substance
- CHLORTHALIDONE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Increased Diuresis [PE], Thiazide-like Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record