Doxycycline
- Product NDC
- 0713-0555
- 11-digit product format
- 007130555
- Labeler code
- 0713
- Product ID
- 0713-0555_d2c8d986-86bf-5528-e053-2a95a90acb28
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Cosette Pharmaceuticals, Inc.
- Application
- ANDA204446
- Marketing category
- ANDA
- Marketing start
- 2015-05-28
- Marketing end
- 2022-10-31
- Substance
- DOXYCYCLINE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0713-0555-50 | 00713055550 | 50 CAPSULE in 1 BOTTLE (0713-0555-50) | 50 capsule | 2017-11-26 | 0000-00-00 | No | No | Current |
| 0713-0555-93 | 00713055593 | 250 CAPSULE in 1 BOTTLE (0713-0555-93) | 250 capsule | 2017-11-26 | 0000-00-00 | No | No | Current |