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Data / Drug companies / Anthea Pharma Private Limited

Anthea Pharma Private Limited: 23 products in the FDA NDC directory, labeler code 83854

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Anthea Pharma Private Limited (labeler code 83854) lists 23 products in the FDA National Drug Code Directory, covering 11 finished drugs by generic name. By type: 23 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on October 14, 2026.

The request: Watch Anthea Pharma Private Limited (FDA labeler code 83854): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
83854
Products in commercial distribution
23
Packages
44
Finished drugs by generic name
11
Prescription products
23
Over the counter products
0
Controlled substance products
Schedule V 1
Flagged as original packager
13 of 13 products that carry the flag
Started marketing in the last 12 months
15
Earliest marketing start
March 21, 2025
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)23100%

Products by type

TypeProductsShare
Prescription drugs23100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

Dosage forms

Dosage formProductsShare
Injection, solution1982.6%
Injection14.3%
Injection, solution, concentrate14.3%
Injection, emulsion14.3%
Injection, powder, lyophilized, for solution14.3%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Fluorescein83854-048InjectionGeneric drugs (ANDA)October 14, 2026
Ketorolac tromethamine83854-024Injection, solutionGeneric drugs (ANDA)September 25, 2026
Ketorolac tromethamine83854-022Injection, solutionGeneric drugs (ANDA)September 25, 2026
Ketrolac tromethamine83854-021Injection, solutionGeneric drugs (ANDA)September 25, 2026
Propofol83854-018Injection, emulsionGeneric drugs (ANDA)July 14, 2026
Bupivacaine Hydrochloride83854-006Injection, solutionGeneric drugs (ANDA)April 22, 2026
Bupivacaine Hydrochloride83854-005Injection, solutionGeneric drugs (ANDA)April 22, 2026
Bupivacaine Hydrochloride83854-004Injection, solutionGeneric drugs (ANDA)April 22, 2026
Bupivacaine Hydrochloride83854-039Injection, solutionGeneric drugs (ANDA)April 21, 2026
Bupivacaine Hydrochloride83854-038Injection, solutionGeneric drugs (ANDA)April 21, 2026
Olanzapine83854-003Injection, powder, lyophilized, for solutionGeneric drugs (ANDA)March 5, 2026
Bumetanide83854-035Injection, solutionGeneric drugs (ANDA)February 27, 2026
Bumetanide83854-007Injection, solutionGeneric drugs (ANDA)February 27, 2026
Lacosamide83854-002Injection, solutionGeneric drugs (ANDA)January 21, 2026
Norepinephrine bitartrate83854-017Injection, solution, concentrateGeneric drugs (ANDA)November 25, 2025
Sodium bicarbonate83854-001Injection, solutionGeneric drugs (ANDA)June 26, 2025
Lidocaine Hydrochloride83854-012Injection, solutionGeneric drugs (ANDA)April 9, 2025
Lidocaine Hydrochloride83854-011Injection, solutionGeneric drugs (ANDA)April 9, 2025
Lidocaine Hydrochloride83854-010Injection, solutionGeneric drugs (ANDA)April 9, 2025
Lidocaine Hydrochloride83854-009Injection, solutionGeneric drugs (ANDA)April 9, 2025
Ropivacaine hydrochloride83854-015Injection, solutionGeneric drugs (ANDA)March 21, 2025
Ropivacaine hydrochloride83854-014Injection, solutionGeneric drugs (ANDA)March 21, 2025
Ropivacaine hydrochloride83854-013Injection, solutionGeneric drugs (ANDA)March 21, 2025

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.