Doxycycline
- Product NDC
- 72789-047
- 11-digit product format
- 727890047
- Labeler code
- 72789
- Product ID
- 72789-047_e71668ac-7b55-3bcb-e053-2995a90a5d5e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA065053
- Marketing category
- ANDA
- Marketing start
- 2000-12-26
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-047 | DOXYCYCLINE CAPSULE [PD-RX PHARMACEUTICALS, INC.] | 17 | Legacy NDC | 20240719_9f200384-d271-46dd-9350-8a71c8d8910a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72789-047-02 | 72789004702 | 2 CAPSULE in 1 BOTTLE, PLASTIC (72789-047-02) | 2 capsule | 2020-01-06 | 0000-00-00 | No | No | Current |