Doxycycline
- Product NDC
- 82804-264
- 11-digit product format
- 828040264
- Labeler code
- 82804
- Product ID
- 82804-264_112c35d6-a397-45de-a57a-6e687cb27b4f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA091605
- Marketing category
- ANDA
- Marketing start
- 2012-05-01
- Substance
- DOXYCYCLINE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC], Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Doxycycline
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DOXYCYCLINE | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | N12000U13O |
| Rxcui | 1650142 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82804-264-20 | Doxycycline | 20 in 1 BOTTLE | TABLET | 20 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-264-20 | 82804026420 | 20 TABLET in 1 BOTTLE (82804-264-20) | 20 tablet | 2026-01-12 | No | No | Current |