Doxycycline
- Product NDC
- 82804-028
- 11-digit product format
- 828040028
- Labeler code
- 82804
- Product ID
- 82804-028_b83c4c4b-2885-43e7-b1c9-0b3bbf75528d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA209582
- Marketing category
- ANDA
- Marketing start
- 2018-01-11
- Substance
- DOXYCYCLINE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC], Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| N12000U13O | DOXYCYCLINE | 17086-28-1 | DOXYCYCLINE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-028-06 | 82804002806 | 6 TABLET, FILM COATED in 1 BOTTLE (82804-028-06) | 2023-10-17 | No | No | Historical |
| 82804-028-14 | 82804002814 | 14 TABLET, FILM COATED in 1 BOTTLE (82804-028-14) | 2023-10-17 | No | No | Historical |
| 82804-028-20 | 82804002820 | 20 TABLET, FILM COATED in 1 BOTTLE (82804-028-20) | 2023-10-17 | No | No | Historical |
| 82804-028-30 | 82804002830 | 30 TABLET, FILM COATED in 1 BOTTLE (82804-028-30) | 2023-10-17 | No | No | Historical |
| 82804-028-60 | 82804002860 | 60 TABLET, FILM COATED in 1 BOTTLE (82804-028-60) | 2023-10-17 | No | No | Historical |
| 82804-028-90 | 82804002890 | 90 TABLET, FILM COATED in 1 BOTTLE (82804-028-90) | 2023-10-17 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Doxycycline Tablets, USP | Proficient Rx LP | 2023-10-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |