TETRA-ABC
- Product NDC
- 43074-103
- 11-digit product format
- 430740103
- Labeler code
- 43074
- Product ID
- 43074-103_255ddf24-7e33-471d-ab91-bc98652e760a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TETRACYCLINE HYDROCHLORIDE
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Phillips Company
- Application
- part333B
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2010-08-24
- Marketing end
- 0000-00-00
- Substance
- TETRACYCLINE HYDROCHLORIDE
- Active strength
- 0 mg/mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 43074-103-01 | TETRA-ABC | 3 mL in 1 BOTTLE, DROPPER | OINTMENT | 3 | | 3 |
| 43074-103-02 | TETRA-ABC | 1 in 1 BOTTLE, PLASTIC | OINTMENT | 1 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43074-103 | TETRA-ABC (TETRACYCLINE HYDROCHLORIDE) OINTMENT [PHILLIPS COMPANY] | 3 | Legacy NDC, 2 package rows | 20100826_9b3c7b34-abd9-417b-a2e9-b7e857339ff5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 43074-103-01 | 43074010301 | 3 mL in 1 BOTTLE, DROPPER | 3 ml | Historical |
| 43074-103-02 | 43074010302 | 1 in 1 BOTTLE, PLASTIC | | Historical |