Doxycycline
- Product NDC
- 68071-4110
- 11-digit product format
- 680714110
- Labeler code
- 68071
- Product ID
- 68071-4110_5abd662a-51e2-8a78-e053-2a91aa0ae06f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline hyclate
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA065095
- Marketing category
- ANDA
- Marketing start
- 2003-07-02
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#