Doxycycline
- Product NDC
- 71335-2638
- 11-digit product format
- 713352638
- Labeler code
- 71335
- Product ID
- 71335-2638_e57b9621-750a-4d3c-b129-f7b0e1e7677d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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
Additional Listing Data
- Finished product
- Yes
- Brand name base
- Doxycycline
- Listing expiration
- 2026-12-31
Active Ingredients
| Ingredient | Strength |
|---|
| DOXYCYCLINE | 100 mg/1 |
Harmonized Identifiers
| Field | Values |
|---|
| Unii | N12000U13O |
| Rxcui | 1650142 |
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 |
|---|
| 71335-2638-1 | 71335263801 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-2638-1) | 2025-06-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Doxycycline Tablets, USP | Bryant Ranch Prepack | 2025-06-02 | HUMAN PRESCRIPTION DRUG LABEL | 1 |