CALCITONIN SALMON
- Product NDC
- 70771-1971
- 11-digit product format
- 707711971
- Labeler code
- 70771
- Product ID
- 70771-1971_6bd84678-423f-47bf-8e46-b128cc690af2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CALCITONIN SALMON
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; SUBCUTANEOUS
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA215864
- Marketing category
- ANDA
- Marketing start
- 2026-04-10
- Substance
- CALCITONIN SALMON
- Active strength
- 200 [USP'U]/mL
- Pharmacologic classes
- Calcitonin [CS], Calcitonin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- CALCITONIN SALMON
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CALCITONIN SALMON | 200 [USP'U]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7SFC6U2VI5 |
| Rxcui | 308866 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70771-1971-1 | CALCITONIN SALMON | 2 mL in 1 VIAL, MULTI-DOSE | INJECTION, SOLUTION | 2 | | 1 |
| 70771-1971-1 | CALCITONIN SALMON | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70771-1971-1 | 70771197101 | 1 VIAL, MULTI-DOSE in 1 CARTON (70771-1971-1) / 2 mL in 1 VIAL, MULTI-DOSE | 2026-04-10 | No | No | Current |