Doxycycline
- Product NDC
- 70771-1007
- 11-digit product format
- 707711007
- Labeler code
- 70771
- Product ID
- 70771-1007_1f788250-9643-4c64-bb4e-4dfefabb8c01
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA209582
- Marketing category
- ANDA
- Marketing start
- 2018-01-11
- Substance
- DOXYCYCLINE
- Active strength
- 75 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 table| Ingredient | Strength |
|---|
| DOXYCYCLINE | 75 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | N12000U13O |
| Rxcui | 1649429, 1650142, 1650444, 1652673 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70771-1007-1 | Doxycycline | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70771-1007 | DOXYCYCLINE TABLET, FILM COATED [ZYDUS LIFESCIENCES LIMITED] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241201_c886b2e4-494a-4325-abaf-981fc3d01c66.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70771-1007-1 | 70771100701 | 100 TABLET, FILM COATED in 1 BOTTLE (70771-1007-1) | 2018-01-11 | 0000-00-00 | No | No | Current |