Doxycycline
- Product NDC
- 43063-682
- 11-digit product format
- 430630682
- Labeler code
- 43063
- Product ID
- 43063-682_7cd7ee74-3c1a-36b9-e053-2991aa0a89d0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, In
- Application
- ANDA204446
- Marketing category
- ANDA
- Marketing start
- 2015-05-28
- Marketing end
- 2019-09-30
- Substance
- DOXYCYCLINE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Tetracycline-cl
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record