Doxycycline
- Product NDC
- 70518-0187
- 11-digit product format
- 705180187
- Labeler code
- 70518
- Product ID
- 70518-0187_df62c3c8-ab97-2b7f-e053-2a95a90a1caa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- doxycycline
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA065055
- Marketing category
- ANDA
- Marketing start
- 2017-01-31
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC], Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0187-1 | 70518018701 | 14 CAPSULE in 1 BOTTLE, PLASTIC (70518-0187-1) | 14 capsule | 2017-03-02 | 0000-00-00 | No | No | Current |