Doxycycline
- Product NDC
- 0713-0571
- 11-digit product format
- 007130571
- Labeler code
- 0713
- Product ID
- 0713-0571_7603372c-888b-43c2-9753-aa38ce0b0ee3
- 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
- 0000-00-00
- Substance
- DOXYCYCLINE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0713-0571 | DOXYCYCLINE CAPSULE [COSETTE PHARMACEUTICALS, INC.] | 2 | Legacy NDC | 20241215_a990e1bd-e126-43eb-84dc-2537a5f0ff94.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0713-0571-01 | 00713057101 | 100 CAPSULE in 1 BOTTLE (0713-0571-01) | 100 capsule | 2021-07-01 | 0000-00-00 | No | No | Current |