DOXYCYCLINE
- Product NDC
- 76519-1206
- 11-digit product format
- 765191206
- Labeler code
- 76519
- Product ID
- 76519-1206_7471f4ee-8e28-f46a-e053-2a91aa0a524e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DOXYCYCLINE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- H.J. Harkins Company, Inc.
- Application
- ANDA065055
- Marketing category
- ANDA
- Marketing start
- 2018-07-27
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76519-1206-6 | DOXYCYCLINE | 60 in 1 VIAL, PLASTIC | CAPSULE | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76519-1206 | DOXYCYCLINE CAPSULE [H.J. HARKINS COMPANY, INC.] | 1 | Legacy NDC, 1 package rows | 20180828_7471f4ee-8e27-f46a-e053-2a91aa0a524e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 76519-1206-6 | 76519120606 | 60 in 1 VIAL, PLASTIC | Historical |